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A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
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Lower Extremity Desmoplastic Malignant Melanoma in Egypt
Reham William Doss1, Sahar Daoud2, Alshimaa Mohamed Abbas Mostafa1
1Department of Dermatology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Indian Journal of Dermatology
|October 6, 2017
Summary
Desmoplastic melanoma (DM) is a rare, non-pigmented cancer that challenges clinical diagnosis due to its varied appearance. This case highlights the importance of histopathology in identifying DM, especially after misdiagnosis of benign conditions.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Desmoplastic melanoma (DM) is a rare, non-pigmented subtype of melanoma.
- Its spindle cell morphology and lack of pigment present diagnostic challenges, mimicking benign tumors, other malignancies, and inflammatory conditions.
- Accurate diagnosis is crucial for appropriate patient management and treatment.
Purpose of the Study:
- To report a case of desmoplastic melanoma presenting as multiple nodular lesions.
- To emphasize the diagnostic difficulties encountered in differentiating DM from other skin conditions.
- To highlight the definitive role of histopathological examination in diagnosing DM.
Main Methods:
- Clinical presentation of a patient with multiple lower extremity nodules after electrocautery.
- Differential clinical diagnoses considered: Kaposi sarcoma, hypertrophic lichen, extensive verruca vulgaris.
- Histopathological examination of lesional biopsies.
Main Results:
- Histopathology revealed spindle-shaped cells.
- Immunohistochemical staining was positive for Melan-A and S100.
- These findings confirmed the diagnosis of desmoplastic melanoma.
Conclusions:
- Desmoplastic melanoma can present atypically, posing a diagnostic challenge.
- Clinical suspicion and thorough histopathological evaluation, including immunohistochemistry, are essential for accurate diagnosis.
- Prompt diagnosis of DM is critical for effective therapeutic strategies.

