Cutaneous CD4+ CD56+ hematologic malignancies.

TitleCutaneous CD4+ CD56+ hematologic malignancies.
Publication TypeJournal Article
Year of Publication2010
AuthorsMagro CM, Porcu P, Schaefer J, Erter JW, Furman RR, Shitabata PK, A Crowson N
JournalJ Am Acad Dermatol
Volume63
Issue2
Pagination292-308
Date Published2010 Aug
ISSN1097-6787
KeywordsAdult, Aged, Biopsy, CD4 Antigens, CD56 Antigen, Dendritic Cells, Fatal Outcome, Hematologic Neoplasms, Humans, Immunophenotyping, Killer Cells, Natural, Leukemia, Myeloid, Acute, Leukemia, T-Cell, Lymphoma, Large B-Cell, Diffuse, Lymphoma, T-Cell, Male, Middle Aged, Mycosis Fungoides, Sarcoma, Myeloid, Skin Neoplasms
Abstract

BACKGROUND: Hematologic malignancies expressing CD4 and CD56 are most commonly associated with the recently described CD4(+) CD56(+) hematodermic neoplasm.

METHODS: Thirteen cases of CD4(+) CD56(+) hematologic malignancies were prospectively encountered in the routine and referral practices of the authors.

RESULTS: Patients 1 and 2 were elderly men exhibiting an acute onset of skin, bone-marrow, and peripheral blood involvement, both dying of their disease within less than 12 months. CD3(+) phenotype and a clonal T-cell receptor beta rearrangement indicated categorization as a CD4(+) natural killer T-cell lymphoma. Patient 3 developed a CD56(+) anaplastic large cell lymphoma and is without disease after excision and radiation. Indolent CD4(+) CD56(+) poikilodermatous mycosis fungoides defined case 4. There were 7 patients with CD123(+) CD4(+) CD56(+) hematodermic neoplasm, 4 dying within 18 months of presentation with peripheral blood/marrow involvement in 6 of the 7 cases. Two patients with granulocytic sarcoma dying within 100 days of presentation defined the last two cases.

LIMITATIONS: There were relatively small numbers in each of the categories and the follow-up was limited in those cases where death was not reported.

CONCLUSION: Cutaneous malignancies composed of CD4(+) CD56(+) hematopoietic cells define a varied group and oftentimes have an aggressive clinical course although not in every case.

DOI10.1016/j.jaad.2009.08.044
Alternate JournalJ Am Acad Dermatol
PubMed ID20541283
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