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DOI: 10.4103/ijmpo.ijmpo_87_17
Epithelioid Sarcoma Presenting as Recurrent Thumb Ulcer: A Lesson to Learn
Autoren
Financial support and sponsorship Nil.
Abstract
Epithelioid sarcoma (ES) first described by Enzinger in 1970,[1] is a rare soft-tissue sarcoma typically presenting as a subcutaneous or deep dermal mass in distal portions of the extremities of adolescents and young adults. They are frequently mistaken for ulcers, abscesses, or infected warts that fail medical management. Patients often develop multiple local recurrences of long duration, with subsequent metastases in 30%–50% of cases.[2] We here report a case of left thumb ES that presented as an ulcer and subsequently metastasized to the forearm, arm, axillary lymph nodes, and lungs.
Publikationsverlauf
Artikel online veröffentlicht:
17. Juni 2021
© 2018. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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References
- 1 Enzinger FM. Epitheloid sarcoma. A sarcoma simulating a granuloma or a carcinoma. Cancer 1970; 26: 1029-41
- 2 Chase DR, Enzinger FM. Epithelioid sarcoma. Diagnosis, prognostic indicators, and treatment. Am J Surg Pathol 1985; 9: 241-63
- 3 Guillou L, Wadden C, Coindre JM, Krausz T, Fletcher CD. “Proximal-type” epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol 1997; 21: 130-46
- 4 Fisher C. Epithelioid sarcoma: The spectrum of ultrastructural differentiation in seven immunohistochemically defined cases. Hum Pathol 1988; 19: 265-75
- 5 Spillane AJ, Thomas JM, Fisher C. Epithelioid sarcoma: The clinicopathological complexities of this rare soft tissue sarcoma. Ann Surg Oncol 2000; 7: 218-25
- 6 Callister MD, Ballo MT, Pisters PW, Patel SR, Feig BW, Pollock RE. et al. Epithelioid sarcoma: Results of conservative surgery and radiotherapy. Int J Radiat Oncol Biol Phys 2001; 51: 384-91
- 7 de Visscher SA, van Ginkel RJ, Wobbes T, Veth RP, Ten Heuvel SE, Suurmeijer AJ. et al. Epithelioid sarcoma: Still an only surgically curable disease. Cancer 2006; 107: 606-12
- 8 Jones RL, Constantinidou A, Olmos D, Thway K, Fisher C, Al-Muderis O. et al. Role of palliative chemotherapy in advanced epithelioid sarcoma. Am J Clin Oncol 2012; 35: 351-7
- 9 Pink D, Richter S, Gerdes S, Andreou D, Tunn PU, Busemann C. et al. Gemcitabine and docetaxel for epithelioid sarcoma: Results from a retrospective, multi-institutional analysis. Oncology 2014; 87: 95-103
- 10 Guillou L, Wadden C, Coindre JM, Krausz T, Fletcher CD. “Proximal-type” epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol 1997; 21: 130-46