Anusha Thangaraja

Anusha Thangaraja

, Bangalore, Karnataka, India

Profile ID RP-000-7697 Joined 2023-06-17 3 articles
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Articles(3)

Authors: Anusha Thangaraja*, Tejaswini B N, Veena Ramaswamy, Sowmya B Uthaiah

DOI: 10.18231/j.ijmpo.2023.015  

Volume9

Issue2

Pages74-76

Abstract

Introduction: Periductal stromal sarcoma (PSS) is a an extremely rare low-grade malignant neoplasm arising from breast periductal stroma. It usually occurs in peri and post-menopausal women. Herein, we report a rare case of a 14 year girl, known case of recurrent Rhabdomyosarcoma (RMS) presenting with periductal stromal sarcoma of breast. To the best of our knowledge, this is a first of its kind to be reported in literature. Case Details: A 14year girl, known case of Recurrent Pleomorphic Rhabdomyosarcoma of retroperitoneum, presented with an abdominal mass and lump in right breast after 10 years. On chemotherapy, abdominal mass regressed and breast lump progressed in size. On further evaluation by histopathological examination and immunohistochemistry, the breast lump turned out to be a periductal stromal sarcoma. Discussion: Periductal stromal tumors have histological similarities to phyllodes tumors, with the biphasic presence of hypercellular and variably atypical, mitotically active stroma hugging benign epithelium. There are very few case reports on periductal stromal tumors and thus a rare entity. PSS as a metachronous presentation with recurrent RMS is even more rare with the prevalence of multiple soft tissue sarcomas being 0.08%. Conclusion: A clinically suspected metastatic lesion, if accessible for biopsy, warrants a meticulous histopathological examination to ascertain the cell of origin. The therapeutic strategy and prognosis of PSS is unclear, thus a longer follow up is imperative to determine its prognosis and clinical outcome. Novelty: 2 case reported so far in younger individuals. 1st case of PSS in a Recurrent RMS.   Keywords: Periductal stromal sarcoma (PSS), Recurrent Rhabdomyosarcoma (RMS), immunohistochemistry (IHC)

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Authors: Anusha Thangaraja*, Veena Ramaswamy, Tejaswini B N, Sowmya B Uthaiah

DOI: 10.18231/j.achr.2023.028  

Volume8

Issue2

Pages123-125

Abstract

Canalicular adenoma is a rare benign salivary gland neoplasm affecting predominantly the minor salivary gland. We present a case of a 55 year female who presented with a mucosal nodule in the left cheek and was diagnosed as Canalicular adenoma based on the morphology and immunohistochemistry findings. Our case is rare in that, it is a case of Canalicular adenoma affecting the major salivary gland – Parotid gland, and is the 7 case reported in literature to the best of our knowledge.   Keywords: Canalicular adenoma, Parotid gland, Immunohistochemsitry

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