Langerhans cell sarcoma involving skin and showing epidermotropism: a comprehensive review

Shira Ronen, Elizabeth Keiser, Katrina M Collins, Phyu P Aung, Priyadharsini Nagarajan, Michael T Tetzlaff, Jonathan L Curry, Doina Ivan, Victor G Prieto, Sharon Hymes, L Jeffrey Medeiros, Carlos A Torres-Cabala

Research output: Contribution to journalArticlepeer-review

Abstract

Langerhans cell sarcoma (LCS) is rare and aggressive and patients have an overall survival rate of less than 50%. We present a 62-year old man with a history of superficial spreading melanoma of the upper back with sentinel lymph node metastasis, Langerhans cell histiocytosis and LCS. The patient presented with erythematous papules and scaly areas on his face, neck, arms, chest, abdomen, and legs. A skin biopsy revealed a proliferation of large neoplastic cells involving the dermis with epidermotropism. These cells had atypical bean-shaped nuclei, with ample cytoplasm and abundant mitotic figures including atypical forms. Immunohistochemical studies showed the tumor to be diffusely positive for CD1a, S100 protein, and langerin (CD207) and negative for melanocytic markers. Some tumor cells were positive for cyclin D1. A diagnosis of LCS involving the skin was established. The present is a very unusual case of LCS showing epidermotropism. The patient's history of metastatic melanoma posed additional challenges for diagnosis, underlying the need of immunophenotyping in these cases. Consensus for optimal standard therapy has not been established in LCS and thus, early recognition is important since these neoplasms tend to recur and metastasize. LCS in skin is discussed and published cases are comprehensively reviewed. This article is protected by copyright. All rights reserved.

Original languageEnglish (US)
JournalJournal of cutaneous pathology
DOIs
StateE-pub ahead of print - Jul 9 2020

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