Melanoma in an Unlikely Guise: Diagnostic Challenges of a Solid–cystic Popliteal Mass in Neurofibromatosis Type 1

ABSTRACT: Malignant melanoma (MM) uncommonly presents as a solid-cystic soft tissue mass, posing a significant diagnostic challenge. We report a rare case in a 63-year-old woman with neurofibromatosis type 1 (NF-1) who presented with a painful, rapidly progressive swelling on the posterior aspect of her right lower thigh. Imaging revealed a large, well-defined solid-cystic lesion suggestive of a soft tissue sarcoma or malignant peripheral nerve sheath tumor. Initial fine-needle aspiration cytology was nondiagnostic. Definitive diagnosis was achieved following wide surgical excision, with histopathological and immunohistochemical analysis confirming MM (strongly positive for S100, Melan-A, and SOX10). This case highlights that MM must be considered in the differential diagnosis of atypical cystic soft tissue lesions, even in anatomically unexpected locations, especially in patients with predisposing conditions such as NF-1 and affirms the indispensable integration of multimodality imaging with histopathological and immunohistochemical correlation in resolving diagnostically challenging soft tissue masses.

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Publication Details

Journal
Annals of African Medicine
Published
2026-06-09
DOI
https://doi.org/10.4103/aam.aam_289_26
Primary Topic
Neurofibromatosis and Schwannoma Cases
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article
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article

Melanoma in an Unlikely Guise: Diagnostic Challenges of a Solid–cystic Popliteal Mass in Neurofibromatosis Type 1

Ankita Pandey, R. Roy, Archana Buch, Purnachandra Lamghare
Annals of African Medicine
Neurofibromatosis and Schwannoma Cases
article

Melanoma in an Unlikely Guise: Diagnostic Challenges of a Solid–cystic Popliteal Mass in Neurofibromatosis Type 1

Ankita Pandey, R. Roy, Archana Buch, Purnachandra Lamghare
article en

Abstract

ABSTRACT: Malignant melanoma (MM) uncommonly presents as a solid-cystic soft tissue mass, posing a significant diagnostic challenge. We report a rare case in a 63-year-old woman with neurofibromatosis type 1 (NF-1) who presented with a painful, rapidly progressive swelling on the posterior aspect of her right lower thigh. Imaging revealed a large, well-defined solid-cystic lesion suggestive of a soft tissue sarcoma or malignant peripheral nerve sheath tumor. Initial fine-needle aspiration cytology was nondiagnostic. Definitive diagnosis was achieved following wide surgical excision, with histopathological and immunohistochemical analysis confirming MM (strongly positive for S100, Melan-A, and SOX10). This case highlights that MM must be considered in the differential diagnosis of atypical cystic soft tissue lesions, even in anatomically unexpected locations, especially in patients with predisposing conditions such as NF-1 and affirms the indispensable integration of multimodality imaging with histopathological and immunohistochemical correlation in resolving diagnostically challenging soft tissue masses.

Annals of African Medicine
Dr. D. Y. Patil Medical College, Hospital and Research Centre (IN), Dr. D.Y. Patil Vidyapeeth, Pune (IN)
Good health and well-being, Gender equality
Openalex Percentile: Top 9%
Neurofibromatosis and Schwannoma Cases
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Melanoma in an Unlikely Guise: Diagnostic Challenges of a Solid–cystic Popliteal Mass in Neurofibromatosis Type 1 — Ankita Pandey, R. Roy, et al. · Annals of African Medicine (2026) | TGRS Research Map | TGRS