DISSEMINATED DERMAL DENDROCYTOMAS - A NEW CUTANEOUS FIBROHISTIOCYTIC PROLIFERATIVE DISORDER

被引:23
作者
NICKOLOFF, BJ
WOOD, GS
CHU, M
BECKSTEAD, JH
GRIFFITHS, CEM
机构
[1] UNIV MICHIGAN,MED CTR,DEPT DERMATOL,ANN ARBOR,MI 48109
[2] VET ADM MED CTR,DEPT PATHOL,PORTLAND,OR 97207
[3] CASE WESTERN RESERVE UNIV,DEPT DERMATOL,CLEVELAND,OH 44106
[4] CASE WESTERN RESERVE UNIV,DEPT PATHOL,CLEVELAND,OH 44106
[5] STANFORD UNIV,MED CTR,DEPT DERMATOL,STANFORD,CA 94305
关键词
Dermal dendrocyte; Factor XIIIa; Immunohistochemistry;
D O I
10.1097/00000478-199009000-00008
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A 77- year-old white woman presented with 1 1/2 -year history of progressively enlarging cutaneous papules, nodules, and plaques, some of which had spontaneously regressed. Her past medical history included untreated chronic lymphocytic leukemia for 10 years' duration. Multiple skin biopsy specimens revealed a diffuse superficial and deep dermal spindle-cell infiltrate accompanied by occasional foamy round cells and multinucleated giant cells. The spindle-shaped cells were focally arranged in a storiform pattern with prominent fibrous stroma. The spindle-shaped cells stained positively for numerous macrophage markers including CD45, factor XIIIa, Leu M5, HLA-DR, CD4, and Leu M3, consistent with dermal dendrocytes. They were also positive for nonspecific esterase and acid phosphatase, which is typical of tissue macrophages. The spindle-shaped cells were negative for CD-1, S-100, and ATPase activity, thus excluding a Langerhans cell immunophenotype. Combining the clinical features, light microscopoy, immunohistochemistry, and enzymatic analysis, this patient appears to represent a novel cutaneous fibrohistiocytic proliferative disorder that features large numbers of dermal dendrocytes.
引用
收藏
页码:867 / 871
页数:5
相关论文
共 22 条
[1]   MULTIPLE DERMATOFIBROMAS IN A PATIENT WITH MYASTHENIA-GRAVIS TREATED WITH PREDNISONE AND CYCLOPHOSPHAMIDE [J].
BARGMAN, HB ;
FEFFERMAN, I .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1986, 14 (02) :351-352
[2]   CHARACTERIZATION OF FACTOR-XIIIA POSITIVE DERMAL DENDRITIC CELLS IN NORMAL AND INFLAMED SKIN [J].
CERIO, R ;
GRIFFITHS, CEM ;
COOPER, KD ;
NICKOLOFF, BJ ;
HEADINGTON, JT .
BRITISH JOURNAL OF DERMATOLOGY, 1989, 121 (04) :421-431
[3]  
CERIO R, 1989, BRIT J DERMATOL, V120, P197
[4]  
ESTRADA JA, 1990, DERMATOLOGICA, V180, P51
[5]   HISTIOCYTIC SYNDROMES - A REVIEW [J].
GIANOTTI, F ;
CAPUTO, R .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1985, 13 (03) :383-404
[6]   CURRENT CONCEPTS - IMMUNOLOGY - MONOCYTES AND MACROPHAGES [J].
JOHNSTON, RB .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (12) :747-752
[7]  
LICHTENSTEIN L, 1953, AMA ARCH PATHOL, V56, P84
[8]   A REAPPRAISAL OF EOSINOPHILIC GRANULOMA OF BONE, HAND-SCHULLER-CHRISTIAN SYNDROME AND LETTERER-SIWE SYNDROME [J].
LIEBERMAN, P ;
JONES, CR ;
DARGEON, HWD ;
BEGG, CF .
MEDICINE, 1969, 48 (05) :375-+
[9]  
MULLER SA, 1987, ARCH DERMATOL, V96, P11
[10]   BRIEF RECORDINGS - MULTIPLE DERMATOFIBROMAS IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS ON IMMUNOSUPPRESSIVE THERAPY [J].
NEWMAN, DM ;
WALTER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1973, 289 (16) :842-843