Particular histological features of a case of Sweet's syndrome induced by G-CSF

被引:5
作者
Abecassis, S
Ingen-Housz-Oro, S [1 ]
Cavelier-Balloy, B
Arnulf, B
Bachelez, H
Dubertret, L
机构
[1] Ctr Hosp Victor Dupony, Serv Dermatol, F-95107 Argenteuil, France
[2] Hop St Louis, Serv Dermatol, F-75010 Paris, France
[3] Hop St Louis, Serv Anat Pathol, F-75010 Paris, France
[4] Hop St Louis, Serv Immunohematol, F-75010 Paris, France
来源
ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE | 2004年 / 131卷 / 04期
关键词
D O I
10.1016/S0151-9638(04)93617-4
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Background. Sweet's syndrome may occur during medullar aplasia, especially after treatment with exogenous growth factors such as G-CSF. In this context, Sweet's syndrome presents particular histological features that we detail in this observation. Case report. A 50 year-old man was treated for multiple myeloma with a mobilizating chemotherapy prior to autologous stem cell transplantation. Four days after the onset of G-CSF, he presented with a febrile generalized eruption of erythematous infiltrated lesions. Histological examination of a skin biopsy showed a neutrophilic infiltrate associated with atypical xanthomized histiocytes and vascular hyperplasia with marked endothelial turgescence.. Treatment with a short cause of oral corticosteroids was efficient. Discussion. The classical histological features of Sweet's syndrome consist in a dermal neutrophilic infiltrate with edema. in our patient, we noticed the presence of atypical histiocytes among the dermal neutrophilic infiltrate. These histiocytes are described in maculo-papular eruptions induced by G-CSF, and should not be confused with a malignant infiltrate associated with a hemopathy. Vascular hyperplasia may be related to the angiogenic properties of G-CSF. Knowledge of these histological features would enable clinicians and histologists to recognize the appropriate diagnosis.
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页码:369 / 372
页数:4
相关论文
共 23 条
[1]
NEUTROPHILIC DERMATOSES DURING GRANULOCYTOPENIA [J].
ARACTINGI, S ;
MALLET, V ;
PINQUIER, L ;
CHOSIDOW, O ;
VIGNONPENNAMEN, MD ;
DEGOS, L ;
DUBERTRET, L ;
DOMBRET, H .
ARCHIVES OF DERMATOLOGY, 1995, 131 (10) :1141-1145
[2]
Bachmeyer C, 1998, BRIT J DERMATOL, V139, P354
[3]
Sweet syndrome in multiple myeloma: a series of six cases [J].
Bayer-Garner, IB ;
Cottler-Fox, M ;
Smoller, BR .
JOURNAL OF CUTANEOUS PATHOLOGY, 2003, 30 (04) :261-264
[4]
INVITRO AND INVIVO ACTIVATION OF ENDOTHELIAL-CELLS BY COLONY-STIMULATING FACTORS [J].
BUSSOLINO, F ;
ZICHE, M ;
WANG, JM ;
ALESSI, D ;
MORBIDELLI, L ;
CREMONA, O ;
BOSIA, A ;
MARCHISIO, PC ;
MANTOVANI, A .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (03) :986-995
[5]
Chao SC, 1997, J FORMOS MED ASSOC, V96, P276
[6]
HISTIOCYTES IN SWEETS SYNDROME [J].
DELABIE, J ;
DEWOLFPEETERS, C ;
MORREN, M ;
MARIEN, K ;
ROSKAMS, T ;
DESMET, V .
BRITISH JOURNAL OF DERMATOLOGY, 1991, 124 (04) :348-353
[7]
Histopathology of cutaneous reaction to granulocyte colony-stimulating factor:: another pseudomalignancy [J].
Fariña, MC ;
Requena, L ;
Dómine, M ;
Soriano, ML ;
Estevez, L ;
Barat, A .
JOURNAL OF CUTANEOUS PATHOLOGY, 1998, 25 (10) :559-562
[8]
SWEETS-SYNDROME DURING THERAPY WITH GRANULOCYTE-COLONY-STIMULATING FACTOR IN A PATIENT WITH APLASTIC-ANEMIA [J].
FUKUTOKU, M ;
SHIMIZU, S ;
OGAWA, Y ;
TAKESHITA, S ;
MASAKI, Y ;
ARAI, T ;
HIROSE, Y ;
SUGAI, S ;
KONDA, S ;
TAKIGUCHI, T .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 86 (03) :645-648
[9]
A generalized cutaneous reaction induced by granulocyte colony-stimulating factor [J].
Glass, LF ;
Fotopoulos, T ;
Messina, JL .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 34 (03) :455-459
[10]
Hasegawa M, 1998, EUR J DERMATOL, V8, P503