Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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On Sep 2018




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Prof. Somashekhar Nimbalkar
Head, Department of Pediatrics, Pramukhswami Medical College, Karamsad
Chairman, Research Group, Charutar Arogya Mandal, Karamsad
National Joint Coordinator - Advanced IAP NNF NRP Program
Ex-Member, Governing Body, National Neonatology Forum, New Delhi
Ex-President - National Neonatology Forum Gujarat State Chapter
Department of Pediatrics, Pramukhswami Medical College, Karamsad, Anand, Gujarat.
On Sep 2018




Dr. Kalyani R

"Journal of Clinical and Diagnostic Research is at present a well-known Indian originated scientific journal which started with a humble beginning. I have been associated with this journal since many years. I appreciate the Editor, Dr. Hemant Jain, for his constant effort in bringing up this journal to the present status right from the scratch. The journal is multidisciplinary. It encourages in publishing the scientific articles from postgraduates and also the beginners who start their career. At the same time the journal also caters for the high quality articles from specialty and super-specialty researchers. Hence it provides a platform for the scientist and researchers to publish. The other aspect of it is, the readers get the information regarding the most recent developments in science which can be used for teaching, research, treating patients and to some extent take preventive measures against certain diseases. The journal is contributing immensely to the society at national and international level."



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Sri Devaraj Urs Medical College
Sri Devaraj Urs Academy of Higher Education and Research , Kolar, Karnataka
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Dr. Saumya Navit

"As a peer-reviewed journal, the Journal of Clinical and Diagnostic Research provides an opportunity to researchers, scientists and budding professionals to explore the developments in the field of medicine and dentistry and their varied specialities, thus extending our view on biological diversities of living species in relation to medicine.
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Professor and Head
Department of Pediatric Dentistry
Saraswati Dental College
Lucknow
On Sep 2018




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Dr. Arunava Biswas
MD, DM (Clinical Pharmacology)
Assistant Professor
Department of Pharmacology
Calcutta National Medical College & Hospital , Kolkata




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Best regards,
C.S. Ramesh Babu,
Associate Professor of Anatomy,
Muzaffarnagar Medical College,
Muzaffarnagar.
On Aug 2018




Dr. Arundhathi. S
"Journal of Clinical and Diagnostic Research (JCDR) is a reputed peer reviewed journal and is constantly involved in publishing high quality research articles related to medicine. Its been a great pleasure to be associated with this esteemed journal as a reviewer and as an author for a couple of years. The editorial board consists of many dedicated and reputed experts as its members and they are doing an appreciable work in guiding budding researchers. JCDR is doing a commendable job in scientific research by promoting excellent quality research & review articles and case reports & series. The reviewers provide appropriate suggestions that improve the quality of articles. I strongly recommend my fraternity to encourage JCDR by contributing their valuable research work in this widely accepted, user friendly journal. I hope my collaboration with JCDR will continue for a long time".



Dr. Arundhathi. S
MBBS, MD (Pathology),
Sanjay Gandhi institute of trauma and orthopedics,
Bengaluru.
On Aug 2018




Dr. Mamta Gupta,
"It gives me great pleasure to be associated with JCDR, since last 2-3 years. Since then I have authored, co-authored and reviewed about 25 articles in JCDR. I thank JCDR for giving me an opportunity to improve my own skills as an author and a reviewer.
It 's a multispecialty journal, publishing high quality articles. It gives a platform to the authors to publish their research work which can be available for everyone across the globe to read. The best thing about JCDR is that the full articles of all medical specialties are available as pdf/html for reading free of cost or without institutional subscription, which is not there for other journals. For those who have problem in writing manuscript or do statistical work, JCDR comes for their rescue.
The journal has a monthly publication and the articles are published quite fast. In time compared to other journals. The on-line first publication is also a great advantage and facility to review one's own articles before going to print. The response to any query and permission if required, is quite fast; this is quite commendable. I have a very good experience about seeking quick permission for quoting a photograph (Fig.) from a JCDR article for my chapter authored in an E book. I never thought it would be so easy. No hassles.
Reviewing articles is no less a pain staking process and requires in depth perception, knowledge about the topic for review. It requires time and concentration, yet I enjoy doing it. The JCDR website especially for the reviewers is quite user friendly. My suggestions for improving the journal is, more strict review process, so that only high quality articles are published. I find a a good number of articles in Obst. Gynae, hence, a new journal for this specialty titled JCDR-OG can be started. May be a bimonthly or quarterly publication to begin with. Only selected articles should find a place in it.
An yearly reward for the best article authored can also incentivize the authors. Though the process of finding the best article will be not be very easy. I do not know how reviewing process can be improved. If an article is being reviewed by two reviewers, then opinion of one can be communicated to the other or the final opinion of the editor can be communicated to the reviewer if requested for. This will help one’s reviewing skills.
My best wishes to Dr. Hemant Jain and all the editorial staff of JCDR for their untiring efforts to bring out this journal. I strongly recommend medical fraternity to publish their valuable research work in this esteemed journal, JCDR".



Dr. Mamta Gupta
Consultant
(Ex HOD Obs &Gynae, Hindu Rao Hospital and associated NDMC Medical College, Delhi)
Aug 2018




Dr. Rajendra Kumar Ghritlaharey

"I wish to thank Dr. Hemant Jain, Editor-in-Chief Journal of Clinical and Diagnostic Research (JCDR), for asking me to write up few words.
Writing is the representation of language in a textual medium i e; into the words and sentences on paper. Quality medical manuscript writing in particular, demands not only a high-quality research, but also requires accurate and concise communication of findings and conclusions, with adherence to particular journal guidelines. In medical field whether working in teaching, private, or in corporate institution, everyone wants to excel in his / her own field and get recognised by making manuscripts publication.


Authors are the souls of any journal, and deserve much respect. To publish a journal manuscripts are needed from authors. Authors have a great responsibility for producing facts of their work in terms of number and results truthfully and an individual honesty is expected from authors in this regards. Both ways its true "No authors-No manuscripts-No journals" and "No journals–No manuscripts–No authors". Reviewing a manuscript is also a very responsible and important task of any peer-reviewed journal and to be taken seriously. It needs knowledge on the subject, sincerity, honesty and determination. Although the process of reviewing a manuscript is a time consuming task butit is expected to give one's best remarks within the time frame of the journal.
Salient features of the JCDR: It is a biomedical, multidisciplinary (including all medical and dental specialities), e-journal, with wide scope and extensive author support. At the same time, a free text of manuscript is available in HTML and PDF format. There is fast growing authorship and readership with JCDR as this can be judged by the number of articles published in it i e; in Feb 2007 of its first issue, it contained 5 articles only, and now in its recent volume published in April 2011, it contained 67 manuscripts. This e-journal is fulfilling the commitments and objectives sincerely, (as stated by Editor-in-chief in his preface to first edition) i e; to encourage physicians through the internet, especially from the developing countries who witness a spectrum of disease and acquire a wealth of knowledge to publish their experiences to benefit the medical community in patients care. I also feel that many of us have work of substance, newer ideas, adequate clinical materials but poor in medical writing and hesitation to submit the work and need help. JCDR provides authors help in this regards.
Timely publication of journal: Publication of manuscripts and bringing out the issue in time is one of the positive aspects of JCDR and is possible with strong support team in terms of peer reviewers, proof reading, language check, computer operators, etc. This is one of the great reasons for authors to submit their work with JCDR. Another best part of JCDR is "Online first Publications" facilities available for the authors. This facility not only provides the prompt publications of the manuscripts but at the same time also early availability of the manuscripts for the readers.
Indexation and online availability: Indexation transforms the journal in some sense from its local ownership to the worldwide professional community and to the public.JCDR is indexed with Embase & EMbiology, Google Scholar, Index Copernicus, Chemical Abstracts Service, Journal seek Database, Indian Science Abstracts, to name few of them. Manuscriptspublished in JCDR are available on major search engines ie; google, yahoo, msn.
In the era of fast growing newer technologies, and in computer and internet friendly environment the manuscripts preparation, submission, review, revision, etc and all can be done and checked with a click from all corer of the world, at any time. Of course there is always a scope for improvement in every field and none is perfect. To progress, one needs to identify the areas of one's weakness and to strengthen them.
It is well said that "happy beginning is half done" and it fits perfectly with JCDR. It has grown considerably and I feel it has already grown up from its infancy to adolescence, achieving the status of standard online e-journal form Indian continent since its inception in Feb 2007. This had been made possible due to the efforts and the hard work put in it. The way the JCDR is improving with every new volume, with good quality original manuscripts, makes it a quality journal for readers. I must thank and congratulate Dr Hemant Jain, Editor-in-Chief JCDR and his team for their sincere efforts, dedication, and determination for making JCDR a fast growing journal.
Every one of us: authors, reviewers, editors, and publisher are responsible for enhancing the stature of the journal. I wish for a great success for JCDR."



Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
Areas for improvement: In certain cases, I felt that the peer review process of the manuscripts was not up to international standards and that it should be strengthened. Also, the number of manuscripts in an issue is high and it may be difficult for readers to go through all of them. The journal can consider tightening of the peer review process and increasing the quality standards for the acceptance of the manuscripts. I faced occasional problems with the online manuscript submission (Pre-publishing) system, which have to be addressed.
Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."



Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Case Series
Year : 2023 | Month : October | Volume : 17 | Issue : 10 | Page : TR01 - TR06 Full Version

Role of Interventional Radiology in the Management of Vascular Lesions around the Knee Joint: A Series of Four Cases


Published: October 1, 2023 | DOI: https://doi.org/10.7860/JCDR/2023/65197.18635
Vishal Nandkishor Bakare, Pratiksha Yadav, Ravi Arya, Ritesh Sahu

1. Assistant Professor, Department of Interventional Radiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India. 2. Head, Department of Interventional Radiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India. 3. Senior Resident, Department of Interventional Radiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India. 4. Senior Resident, Department of Interventional Radiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India.

Correspondence Address :
Dr. Pratiksha Yadav,
Head, Department of Interventional Radiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India.
E-mail: yadavpratiksharit@gmail.com; yadavpratiksha@hotmail.com

Abstract

The soft tissue lesions around the knee range from congenital, traumatic, and vascular to neoplastic in aetiology. The various imaging modalities employed for diagnostic work-up include plain radiographs, ultrasonography, Computed Tomography (CT) scan, and Magnetic Resonance Imaging (MRI). Based on the peculiar imaging findings, the differential diagnosis can be narrowed down; however, the final diagnosis relies on histopathological findings. Some of the highly vascular lesions are arteriovenous malformation, malignant fibrous histiocytoma, haemangiopericytoma, and synovial sarcoma. The abundant neovascularity within these lesions poses a major problem during surgery due to potential blood loss. Presurgical interventional management in the form of endovascular embolisation significantly reduces intraoperative blood loss. Here, four different cases, one of each type, presenting as highly vascular lesions around the knee joint, were successfully managed with endovascular embolisation.

Keywords

Embolisation, Haemangiopericytoma, Malignant fibrous histiocytoma, Synovial sarcoma, Venous malformation

Lesions around the knee can have varying underlying aetiologies. Among them, highly vascular lesions include arteriovenous malformations, haemangioendothelioma, haemangiopericytoma, malignant fibrous histiocytoma, synovial sarcoma, rhabdomyosarcoma, and angiosarcoma. For the treatment of these lesions, surgery has been the standard approach for many years (1). However, new endovascular techniques have been introduced and have proven to be as effective as open surgery. Recently, their usage has been increasing (1). Due to the rich neovascularity within these lesions, they are prone to repeated bleeding with mild trauma and during surgery. Therefore, presurgical interventional management in the form of endovascular embolisation significantly reduces perioperative blood loss and patient morbidity (1).

Case Report

Case 1

Synovial sarcoma: A 22-year-old female patient presented with complaints of painful swelling in the posterior aspect of her left knee for the past eight months. On clinical examination, the swelling measured approximately 5×5 cm and was located on the posterior aspect of the left knee joint, with prominent superficial veins. There was no significant limitation in the movement of the knee joint. Palpation of the swelling revealed warmth and tenderness. The peripheral pulses of the posterior tibial and dorsalis pedis arteries were weak, but there was no neurological deficit.

A lateral view radiograph showed soft tissue swelling (Table/Fig 1). Ultrasound (US) revealed a predominantly hypoechoic lesion (Table/Fig 2)a with significant vascularity on Doppler (Table/Fig 2)b, along with encasement of the popliteal artery (Table/Fig 2)c,d. MRI revealed a heterogeneous signal intensity lesion. On the T1W sequence, it appeared nearly isointense to the adjacent muscles (Table/Fig 3)a. On the T2W sequence, the lesion exhibited a central hyperintense necrotic component (Table/Fig 3)b. There were no haemorrhages or calcifications within the lesion on the gradient echo sequence (Table/Fig 3)c. On T1W fat-suppressed images, the lesion appeared predominantly hyperintense compared to the surrounding muscles (Table/Fig 3)d. Post-gadolinium fat-suppressed T1W sequences (Table/Fig 3)e revealed heterogeneous enhancement of the lesion, with a non enhancing central necrotic component and no obvious intra-articular extension.

Preoperative embolisation: Retrograde left femoral arterial access was achieved using a 5F vascular sheath. A catheter-guide wire combination was used, and a crossover was performed at the aortic bifurcation to gain access to the left Superficial Femoral Artery (SFA). Angiograms were taken, revealing displacement of the distal popliteal artery and its bifurcation by the lesion. Multiple branches from the popliteal artery, including the anterior and posterior tibial arteries and peroneal artery, were found to supply the lesion (Table/Fig 4)a, resulting in multiple sites of abnormal vascular blush. Embolisation was carried out using 100-micron Polyvinyl Alcohol particles (PVA) through a coaxial 2.9F microcatheter via transarterial access. A final check angiogram was performed with the catheter tip in the distal SFA, showing a significant reduction in the abnormal vascular blush (Table/Fig 4)b, along with patent and densely filling anterior and posterior tibial as well as peroneal arteries (Table/Fig 4)c, indicating the absence of arteriovenous shunting within the lesion. A repeat US examination the following day (Table/Fig 5) revealed a significant reduction in the vascularity of the lesion. The lesion was excised with an intraoperative blood loss of approximately 800 mL. The histopathological diagnosis confirmed synovial sarcoma with a predominant mesenchymal element in the form of spindle cells after biopsy. The patient underwent postsurgery radiotherapy and remained asymptomatic during a three-month follow-up period.

Case 2

Haemangiopericytoma: A 30-year-old female patient presented with complaints of pain and swelling in the left popliteal region for 5-6 months. There was no history of trauma. On clinical examination, the swelling measured approximately 10×5 cm and was located on the posterior aspect of the left knee joint. There was a mild limitation in the movement of the joint, and mild tenderness was present upon palpation. The peripheral pulses of the posterior tibial and dorsalis pedis arteries were normal.

Radiographs revealed abnormal soft tissue density in the popliteal region with no bony abnormalities (Table/Fig 6). US showed an irregular, heterogeneous, predominantly hypoechoic lesion, which encased and displaced the distal popliteal artery and its branches. Significant vascularity within the lesion was observed on Doppler examination (Table/Fig 7). CT angiography was performed, revealing a large, heterogeneous, intensely enhancing mass that encased and displaced the popliteal vessels. However, the vessels remained patent, and there was normal contrast filling of the Anterior Tibial Artery (ATA), Posterior Tibial Artery (PTA), and peroneal arteries (Table/Fig 8). Due to the tumour vascularity, the patient was referred for preoperative embolisation. The transarterial embolisation procedure performed in this case was similar to the aforementioned case (Table/Fig 9)a,b. The embolisation agent used was 100-micron PVA via transarterial access.

The intraoperative blood loss was approximately 650 mL. Histopathological examination of the operative specimen confirmed the diagnosis of haemangiopericytoma. The patient received radiotherapy postoperatively. After six months of follow-up, an MRI revealed postoperative changes without any recurrence (Table/Fig 10).

Case 3

Malignant fibrous histiocytoma: A 28-year-old female presented to the emergency department with active bleeding from a tumour lesion around the right knee joint, following minor trauma. The lesion had been present for one year, slowly growing. The bleeding continued despite the application of a tight compression bandage. Detailed history revealed a diagnosed case of malignant fibrous histiocytoma. On clinical examination, the swelling measured approximately 8×5 cm and was ulcerated, with active bleeding from one site. Joint movements were restricted, and tenderness was present. Knee joint effusion was also observed.

The transarterial embolisation procedure performed in this case was similar to the aforementioned case (Table/Fig 11). The embolisation agent used was a mixture of Lipiodol and n-butyl cyanoacrylate glue in a 2:1 proportion, along with PVA particles, administered via transarterial access. A repeat US examination was performed one week after embolisation, revealing a significant reduction in vascular spaces and a decrease in the size of the swelling. The patient was then started on radiotherapy without any further episodes of bleeding.

Case 4

Venous malformation: A 23-year-old male patient presented with complaints of pain and swelling in the right lower thigh for three years. The swelling gradually increased in size. On clinical examination, the swelling was observed in the supra-patellar region of the right lower thigh, measuring approximately 6×8 cm. Upon palpation, it was partially compressible and reducible in size with a refill upon pressure release. There was no significant limitation in the movement of the knee joint, and the peripheral pulses of the posterior tibial and dorsalis pedis arteries were normal.

An X-ray revealed abnormal soft tissue density in the suprapatellar region (Table/Fig 12). US revealed a lesion with multiple compressible vascular spaces (Table/Fig 13)a,b, showing internal low peak systolic velocity blood flow. MRI showed a relatively well-defined lobulated, heterogeneous signal intensity lesion involving the inferior-medial aspect of the thigh. The lesion displaced the adjacent muscles and appeared hyperintense to muscle on T1W (Table/Fig 14)a, hyperintense on T2W (Table/Fig 14)b and fat-suppressed T1W sequences (Table/Fig 14)c, with the presence of multiple signal voids. The lesion also showed some hyperintense fatty components on the T1W sequence. Post-gadolinium scan revealed strong enhancement (Table/Fig 14)d, with retention of the contrast on a 30-minute delayed scan (Table/Fig 14)e. Based on these imaging findings, the diagnosis of venous malformation was confirmed.

Preoperative embolisation: Under US guidance, the vascular spaces inside the lesion were punctured using a 22G scalp vein set. Retrograde free flow of blood was ensured, indicating the position of the needle tip within the vascular spaces. Slow injection of Sodium tetradecyl sulfate (30 mg/mL) mixed with a contrast agent was performed under fluoroscopic guidance into the cannulated vascular spaces (Table/Fig 15). These steps were repeated until most of the vascular spaces were cannulated and embolised. A repeat US examination one week postembolisation revealed a significant reduction in patent vascular spaces and a decrease in the overall vascularity of the swelling (Table/Fig 16).

Discussion

Synovial sarcoma: Synovial sarcomas are malignant tumours commonly seen in adolescents and young adults. About 60% of synovial sarcomas are localised in the lower limbs. The incidence is usually 0.81-1.42 (2). Their development is typically extra-articular. They can be found anywhere in the body (10% of all soft tissue tumours), but most of them arise in the extremities, particularly near the knee joints (2). The characteristic finding on imaging is the presence of intratumoural calcification or ossification (3). Angiography prior to definitive surgery helps differentiate the lesion, evaluate tumour vessels, and prevent bleeding through embolisation (4). Surgery is the treatment modality of choice, but the tumour often recurs even after wide resection (3). The prognosis of synovial sarcoma is poor, with almost always recurring and five-year survival rates ranging from 25 to 50% depending on the series (2). The general principles of transarterial embolisation treatment involve hindering or reducing blood flow to the tumour, resulting in tumour reduction or destruction. This is achieved by injecting embolic agents into the arteries that supply blood to the tumour (2). Embolisation may be used alone or in combination with other treatments such as surgery, radiation therapy, or systemic therapy (2).

Vascular malformations: Vascular malformations encompass a wide range of anomalies, for which different classification systems have been proposed over time. The important one is given by the International Society for the Study of Vascular Anomalies (ISSVA), based on cellular features, flow characteristics, and clinical behaviour (5). These lesions, though congenital, are usually asymptomatic at birth and become symptomatic later in adolescence or adult life due to rapid growth, vascular engorgement caused by thrombosis, trauma, infection, or hormonal fluctuations. Symptoms may include ulceration, haemorrhage, cardiac failure, and unwanted cosmetic consequences (6). Various imaging modalities, such as radiography, Doppler US, CT scan, and MRI, are used, with MRI playing a pivotal role (6). Angiography is helpful for anatomical assessment and direct puncture of the nidus, which can evaluate the volume and flow pattern of these lesions (6). Endothelial cells play a role in vascular remodeling, especially at the venous stump, which recruits collateral flow. Interventional techniques involve the use of therapeutic agents targeting the venous stump while avoiding harm to adjacent tissue (7).

Haemangiopericytoma: Haemangiopericytoma is a highly vascular tumour that can be found anywhere in the body where there are capillaries. The cell of origin is the pericytes, contractile spindle cells that surround capillaries and post capillary venules (8). It is more common in middle-aged individuals (9). The lower extremity is affected in 35% of cases. It typically presents as an asymptomatic mass or may cause pressure symptoms if it is large enough (8). Haemangiopericytoma is a highly vascular tumour with clinically significant arteriovenous shunting. Angiographically, the typical feature of haemangiopericytoma is a hypervascular lesion with a few feeder arteries that enter the mass, along with radially arranged branching vessels around and inside the tumour. Longstanding, well-demarcated tumour staining and early opacification of veins due to arteriovenous shunting are also observed [10,11]. Smith RB et al., reported the use of preoperative arterial embolisation in the management of a large pelvic haemangiopericytoma that was previously considered unresectable (12). Surgery is the treatment of choice, but local recurrence is not uncommon.

Malignant Fibrous Histiocytoma (MFH): MFH is predominantly seen between the 6th and 7th decades of age (13). The most common site of origin is the extremities (13). MFH can be a primary tumour or can arise secondarily at sites of previous radiation therapy, surgery, fractures, osteonecrosis, Paget’s disease, chronic osteomyelitis, and various benign bony lesions such as fibrous dysplasia, enchondroma, non ossifying fibroma, etc. (14). Primary MFH can arise from the soft tissue or bones. On angiography, the lesion shows diffuse neovascularity with multiple areas retaining the stain and arteriovenous shunting. Clinical and radiological features of vascular lesions around the knee joint are discussed in (Table/Fig 17).

Role of preoperative embolisation: Successful preoperative embolisation is defined as catheterisation of the tumour-supplying arteries with obliteration of more than 70% of the tumour stain. The goal of preoperative embolisation is to exclude the tumour capillary bed, not just the major arterial feeders. Preoperative embolisation helps reduce intraoperative blood loss, improves visualisation during surgery, and facilitates en-bloc resection (15).

In a study by Jha R et al., preoperative embolisation of bone tumours was found to be a safe and effective adjunct to the surgical management of primary bone tumours, resulting in a reduction in intraoperative blood loss and transfusion volume (16). Manke C et al., reported a significant reduction in intraoperative haemorrhage in patients who underwent preoperative embolisation for spinal metastases from renal cancer using PVA particles, compared to patients who underwent surgery alone (17). Kickuth R et al., also reported significantly reduced intraoperative blood loss ranging from 200-4000 mL in patients who underwent preoperative embolisation for bone tumours (18). Wong SJ et al., found that intraoperative blood loss ranged from 150 mL to 6,900 mL, with a mean of 1,173 mL and a median of 500 mL in patients who underwent preoperative embolisation for musculoskeletal tumours (15).

Other advantages of preoperative embolisation include a reduction in the amount of viable tumour, a decrease in the rate of tumour growth, and a potential reduction in the need for radiotherapy and chemotherapy (13). Tumour embolisation can also be performed as a standalone procedure in a palliative setting for pain relief (17), reduction of tumour volume (18), or in combination with ablation/cementoplasty (19). Major complications following preoperative tumour embolisation are rare. The most common complications observed are non target embolisation and postembolisation syndrome (20).

Conclusion

Embolisation for highly vascular musculoskeletal lesions is feasible, safe, and highly effective as a primary treatment modality and also as a preparation for definitive surgery. Preoperative embolisation helps reduce intraoperative blood loss, improves visualisation during surgery, and facilitates en-bloc resection. Further large scale studies are needed to validate these results.

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DOI and Others

DOI: 10.7860/JCDR/2023/65197.18635

Date of Submission: May 03, 2023
Date of Peer Review: Aug 07, 2023
Date of Acceptance: Sep 22, 2023
Date of Publishing: Oct 01, 2023

AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: May 10, 2023
• Manual Googling: Sep 16, 2023
• iThenticate Software: Sep 19, 2023 (7%)

ETYMOLOGY: Author Origin

EMENDATIONS: 6

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