Invasive Cystic Hypersecretory Carcinoma of Breast: A Rare and Under Diagnosed Variant of Ductal Carcinoma
Published: June 1, 2017 | DOI: https://doi.org/10.7860/JCDR/2017/27937.10098
Nibedita Sahoo, Pritinanda Mishra, Susama Patra, Prakash Kumar Sasmal
1. Senior Resident, Department of Pathology, AIIMS, Bhubaneswar, Odisha, India.
2. Associate Professor, Department of Pathology, AIIMS, Bhubaneswar, Odisha, India.
3. Professor, Department of Pathology, AIIMS, Bhubaneswar, Odisha, India.
4. Assistant Professor, Department of Surgery, AIIMS, Bhubaneswar, Odisha, India.
Correspondence
Dr. Susama Patra,
Professor, Department of Pathology, AIIMS, Bhubaneswar-761019, Odisha, India.
E-mail: wususama@gmail.com
Handful cases of invasive Cystic Hypersecretory Ductal Carcinoma (CHC) have been reported so far in literature. Cystic hypersecretory lesions of breast have a spectrum of morphological features ranging from Cystic Hypersecretory Hyperplasia (CHH), CHH with atypia, in situ to invasive CHC. We are reporting a case of a 32-year-old female who had nipple discharge and lump in her right breast for one month. A modified radical mastectomy was done and morphological diagnosis of invasive CHC with axillary node metastasis was made. The postoperative events were uneventful. Invasive CHC being a rare entity, our understanding of its biological behavior, prognostic factors and genetic basis is limited. The authors are aware of only 15 similar cases being reported in the English literature.
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