Abstract | BACKGROUND: Regressing atypical histiocytosis is a recently described disease characterized by recurrent nodules or ulcers. The cutaneous lesions appear abruptly and then regress only to return in a manner reminiscent of lymphomatoid papulosis. Immunophenotypic analysis has revealed that most cases are a form of anaplastic large-cell Ki-1-positive (CD30+) lymphoma. OBJECTIVE: METHODS: The clinical and histopathologic findings were recorded. In addition, T-cell receptor gene rearrangement and immunophenotyping were determined in the index case. RESULTS: CONCLUSION: Regressing atypical histiocytosis may clinically resemble some benign dermatoses. Recent evaluation of these cases has shown that many represent a form of Ki-1-positive anaplastic large-cell lymphoma. Multiple skin biopsy specimens with immunophenotyping and gene rearrangement studies are required to arrive at the diagnosis.
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Authors | C Camisa, T N Helm, C Sexton, R Tuthill |
Journal | Journal of the American Academy of Dermatology
(J Am Acad Dermatol)
Vol. 29
Issue 5 Pt 1
Pg. 696-700
(Nov 1993)
ISSN: 0190-9622 [Print] United States |
PMID | 8227541
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Ki-1 Antigen
- Vincristine
- Doxorubicin
- Cyclophosphamide
- Prednisone
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Topics |
- Adult
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Biopsy
- Cyclophosphamide
(administration & dosage)
- Diagnosis, Differential
- Diagnostic Errors
- Doxorubicin
(administration & dosage)
- Female
- Gene Expression
- Gene Rearrangement, T-Lymphocyte
- Humans
- Immunophenotyping
- Ki-1 Antigen
(analysis)
- Lymphoma, Large-Cell, Anaplastic
(diagnosis, drug therapy, immunology)
- Male
- Middle Aged
- Prednisone
(administration & dosage)
- Pyoderma Gangrenosum
(diagnosis)
- Scleroderma, Localized
(diagnosis)
- Skin
(pathology)
- Time Factors
- Vincristine
(administration & dosage)
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