Aseptic abscesses -: A study of 30 patients with or without inflammatory bowel disease and review of the literature

被引:119
作者
Andre, Marc F. J.
Piette, Jean-Charles
Kemeny, Jean-Louis
Ninet, Jacques
Jego, Patrick
Delevaux, Isabelle
Wechsler, Bertrand
Weiller, Pierre-Jean
Frances, Camille
Bletry, Olivier
Wismans, Pieter J.
Rousset, Hugues
Colombel, Jean-Frederic
Aumaitre, Olivier
机构
[1] CHU Clermont Ferrand, Hop Gabriel Montpied, Serv Med Interne, F-63003 Clermont Ferrand, France
[2] CHU Clermont Ferrand, Hop Gabriel Montpied, Serv Anat & Cytol Pathol, F-63003 Clermont Ferrand, France
[3] INSERM, U384, Clermont Ferrand, France
[4] Hop La Pitie Salpetriere, Assistance Publ Hop Paris, Serv Med Interne, Paris, France
[5] Hop Edouard Herriot, Hop Lyon, Serv Med Interne, Lyon, France
[6] CHU Rennes, Serv Med Interne, Hop Sud, Rennes, France
[7] CHU Marseilles, Hop Timone, Serv Med Interne, Marseille, France
[8] Assistance Publ Hop Paris, Hop Tenon, Dermatol Serv, Paris, France
[9] Hop Foch, Serv Med Interne, Suresnes, France
[10] Ctr Hosp Lyon Sud, Serv Med Interne, Pierre Benite, France
[11] CHU Lille, Hop Claude Huriez, Serv Hepato Gastro Enterol, F-59037 Lille, France
[12] INSERM, F-59045 Lille, France
[13] Havenziekenhuis, Afd Interne Geneeskunde, Rotterdam, Netherlands
[14] Inst Trop Ziekten, Rotterdam, Netherlands
关键词
RECURRENT MULTIFOCAL OSTEOMYELITIS; ERYTHEMA-ELEVATUM-DIUTINUM; PYODERMA-GANGRENOSUM; CROHNS-DISEASE; ULCERATIVE-COLITIS; SWEETS-SYNDROME; NEUTROPHILIC DERMATOSIS; RHEUMATOID-ARTHRITIS; SUBCUTANEOUS ABSCESS; BEHCETS-DISEASE;
D O I
10.1097/md.0b013e18064f9f3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aseptic abscesses (AA) are characterized by deep, sterile, round lesions consisting of neutrophil that do not respond to antibiotics but improve dramatically with corticosteroids. We report the clinical, laboratory, and radiologic characteristics and the associated conditions of 29 patients from the French Register on AA plus 1 patient from the Netherlands. The mean age of patients at AA diagnosis was 29 years (SD 14). The main clinical manifestations of AA were fever (90%), abdominal pain (67%), and weight loss (50%). Duration of symptoms was 4.7 months on average until abscesses were discovered. The abscesses involved the spleen in 27/29 patients (93%; the thirtieth patient had a personal history of splenectomy after a trauma). In 7 they were unifocal and in the others they were multifocal, involving in addition the abdominal lymph nodes in 14 (48%), liver in 12 (40%), lung in 5 (17%), pancreas in 2 (7%), and brain in 2 (7%). They were not splenic in 3, including 2 with abdominal lymph nodes and 1 with superficial lymph nodes and testicle and lung involvement. Twenty-two patients (70%) had elevated white blood cell and neutrophil count; antineutrophil cytoplasmic autoantibodies with a perinuclear, cytoplasmic or atypical pattern (negative for antiprotemase 3 and negative for antimyeloperoxidase except for 1) were positive in 21% of the 24 patients tested. Twenty-one patients had inflammatory bowel disease (IBD), which preceded the occurrence of abscesses in 7, was concomitant in 7, and appeared secondarily in 7. Six patients had neutrophilic dermatosis (20%), 3 had relapsing polychondritis as an associated condition, and 3 others had monoclonal gammopathy of undetermined significance. Three patients had no associated condition. Splenectomy was performed in 15 (52%) patients. All patients received steroid therapy. Thirteen (43%) were given additional immunosuppressive therapy, 1 immediately and the others after a relapse, of whom 3 were also treated by anti-tumor necrosis factor-alpha agents. Mean follow-up was 7 years. Eighteen (60%) patients experienced 1 or several relapses, but there was no death related to AA. Relapses occurred on immunosuppressive therapy in 2 patients and off immunosuppressive therapy in the others while corticosteroids were being tapered. We surveyed the literature and analyzed 19 additional cases. AA is an emergent and probably underrecognized entity. It represents an apparently noninfectious inflammatory disorder involving neutrophils that responds to corticosteroid therapy. AA mainly affects patients with IBD but also affects those with other conditions, or with no other apparent disease.
引用
收藏
页码:145 / 161
页数:17
相关论文
共 65 条
[21]   Infliximab for the treatment of metastatic hepatic and pulmonary Crohn's disease [J].
Gill, KRS ;
Mahadevan, U .
INFLAMMATORY BOWEL DISEASES, 2005, 11 (02) :210-212
[22]   IS THE PATHOGENESIS OF SWEETS SYNDROME MEDIATED BY INTERLEUKIN-I [J].
GOING, JJ .
BRITISH JOURNAL OF DERMATOLOGY, 1987, 116 (02) :282-283
[23]   Erythema elevatum diutinum -: evidence for disease-dependent leucocyte alterations and response to dapsone [J].
Grabbe, J ;
Haas, N ;
Möller, A ;
Henz, BM .
BRITISH JOURNAL OF DERMATOLOGY, 2000, 143 (02) :415-420
[24]   Subcutaneous abscesses in a patient with ulcerative colitis [J].
Hara, H ;
Wakui, F ;
Fujitsuka, A ;
Ochiai, T ;
Morishima, T .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (02) :363-365
[25]   Pyoderma gangrenosum with hepatopancreatic manifestations in a patient with rheumatoid arthritis [J].
Hastier, P ;
CaroliBosc, FX ;
Bartel, HR ;
Harris, AG ;
Maes, B ;
Arpurt, JP ;
Taillan, B ;
Bodock, I ;
Dumas, R ;
Delmont, JP .
DIGESTIVE DISEASES AND SCIENCES, 1996, 41 (03) :594-597
[26]   Rheumatoid-like nodules in the spleen: New extraintestinal manifestation of Crohn's disease? [J].
Holstein, A ;
Egberts, EH ;
Von Herbay, A .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2006, 21 (01) :295-298
[27]   Abscess-forming neutrophilic dermatosis: Report of three cases associated with hemopathies [J].
Horiguchi, Y ;
Lee, SG ;
Matsumoto, I ;
Arima, N ;
Fujii, H ;
Ohnuma, Y ;
Imamura, S .
DERMATOLOGY, 1998, 197 (02) :174-177
[28]   PULMONARY NECROBIOTIC NODULES AS A PRESENTING FEATURE OF RHEUMATOID-ARTHRITIS [J].
HULL, S ;
MATHEWS, JA .
ANNALS OF THE RHEUMATIC DISEASES, 1982, 41 (01) :21-24
[29]   THE SAPHO SYNDROME [J].
KAHN, MF ;
KHAN, MA .
BAILLIERES CLINICAL RHEUMATOLOGY, 1994, 8 (02) :333-362
[30]   Multiple pulmonary nodules in association with pyoderma gangrenosum [J].
Kasuga, I ;
Yanagisawa, N ;
Takeo, C ;
Koga, M ;
Kiyokawa, H ;
Yonemaru, M ;
Ichinose, Y ;
Toyama, K .
RESPIRATORY MEDICINE, 1997, 91 (08) :493-495