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CD34 expression in desmoplastic melanoma
Author(s) -
Hoang Mai P.,
Selim M. Angelica,
Bentley Rex C.,
Burchette James L.,
Shea Christopher R.
Publication year - 2001
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1034/j.1600-0560.2001.281003.x
Subject(s) - pathology , melanoma , cd34 , dermatofibrosarcoma protuberans , nuclear atypia , epithelioid cell , biology , immunohistochemistry , pleomorphism (cytology) , s100 protein , medicine , cancer research , stem cell , microbiology and biotechnology
Background: Primary and metastatic malignant melanoma can simulate various soft tissue tumors, including dermatofibrosarcoma protuberans (DFSP). Expression of CD34, a marker characteristic of DFSP, as well as other spindle cell tumors, has not been previously documented in malignant melanoma. Methods: We present here an unusual case of metastatic malignant melanoma with a strong histologic resemblance to DFSP and also CD34 expression. Results: The patient, a 72‐year‐old man with a history of an invasive malignant melanoma of the skin of the right lower abdomen, presented with a right axillary mass. Histologic sections revealed intersecting fascicles of spindle cells with nuclear pleomorphism and numerous mitotic figures, diffusely infiltrating the adipose tissue in a pattern closely simulating that seen in DFSP. In other foci, epithelioid neoplastic cells with abundant cytoplasm, prominent nucleoli, nuclear pseudoinclusions, and focal cytoplasmic melanin pigment were seen. The neoplastic spindle cells were strongly labeled by two anti‐CD34 monoclonal antibodies. Some of the spindle cells and the majority of the epithelioid neoplastic cells expressed S‐100 protein and focally tyrosinase. The tumor cells were negative for HMB‐45 and MART‐1. Melanosomes were not identified by electron microscopy. Conclusion: This case demonstrates the potential of melanoma to simulate DFSP closely, on both morphologic and immunohistochemical grounds, and confirms the utility of employing a broad panel of immunohistochemical reagents in problematic cases.