ANGIOFOLLICULAR LYMPH-NODE HYPERPLASIA (CASTLEMANS DISEASE)

被引:107
作者
MCCARTY, MJ
VUKELJA, SJ
BANKS, PM
WEISS, RB
机构
[1] BROOKE ARMY MED CTR, DEPT MED, HEMATOL ONCOL SERV, FT SAM HOUSTON, TX 78234 USA
[2] UNIV TEXAS, HLTH SCI CTR, DEPT PATHOL, SAN ANTONIO, TX 78284 USA
[3] WALTER REED ARMY MED CTR, DEPT MED, MED ONCOL SECT, WASHINGTON, DC 20307 USA
关键词
D O I
10.1016/0305-7372(95)90034-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This review provides a comprehensive assessment of angiofollicular lymph node hyperplasia (ALNH) or Castleman's disease including pathogenesis, clinical presentation, histomorphologic and immunophenotypic findings, laboratory results, treatment, and prognoses. A division of ALNH into clinically relevant subtypes provides a framework for the consideration of the disorder. A comprehensive search of the medical literature involving ALNH using Medline was performed. Reports judged to be significant for the understanding of the disorder were analyzed and their findings incorporated into this review. ALNH is divided into localized/unicentric ALNH and generalized/multicentric ALNH due to the profound clinical differences seen between these variants. Localized/unicentric ALNH is separated by clinical and histomorphologic criteria into hyaline-vascular (HV) and plasma-cell (PC) subtypes. Generalized/multicentric ALNH may be divided by clinical criteria into generalized/multicentric ALNH without neuropathy (non-neuropathic) and generalized/multicentric ALNH with neuropathy (POEMS-associated or neuropathic). The dichotomy between these two subtypes is not absolute, with considerable clinical overlap occurring among patients presenting with generalized disease. Immunophenotypic and molecular probe studies demonstrate clonal B-cell lymphocyte populations in some cases, particularly those with generalized/multicentric ALNH. However, the finding of clonal populations is of no value in predicting malignant clinical progression. We conclude that using th is division of ALNH, patients presenting with symptoms and histomorphology consistent with ALNH can be subdivided into the appropriate category of ALNH. Localized or unicentric disease, either HV or PC subtype, has an excellent prognosis with surgery being curative in the majority of cases, Generalized or multicentric disease indicates a poor prognosis with short survival, with the neuropathic variant possessing resistance to steroids and chemotherapy and a corresponding worse prognosis.
引用
收藏
页码:291 / 310
页数:20
相关论文
共 126 条
[1]  
ABELL MR, 1957, ARCH PATHOL, V64, P584
[2]   PLASMA-CELL DYSCRASIA WITH POLYNEUROPATHY, ORGANOMEGALY, ENDOCRINOPATHY, M PROTEIN, AND SKIN CHANGES - THE POEMS SYNDROME - REPORT ON 2 CASES AND A REVIEW OF THE LITERATURE [J].
BARDWICK, PA ;
ZVAIFLER, NJ ;
GILL, GN ;
NEWMAN, D ;
GREENWAY, GD ;
RESNICK, DL .
MEDICINE, 1980, 59 (04) :311-322
[3]  
BARTOLI E, 1980, AM J CLIN PATHOL, V73, P423
[4]   GIANT LYMPH-NODE HYPERPLASIA (CASTLEMANS DISEASE) - A CLINICAL-STUDY OF 8 PATIENTS [J].
BARUCH, Y ;
BENARIE, Y ;
KERNER, H ;
LORBER, M ;
BEST, LA ;
GERSHONIBARUCH, R .
POSTGRADUATE MEDICAL JOURNAL, 1991, 67 (786) :366-370
[5]   ALLEVIATION OF SYSTEMIC MANIFESTATIONS OF CASTLEMANS DISEASE BY MONOCLONAL ANTI-INTERLEUKIN-6 ANTIBODY [J].
BECK, JT ;
HSU, SM ;
WIJDENES, J ;
BATAILLE, R ;
KLEIN, B ;
VESOLE, D ;
HAYDEN, K ;
JAGANNATH, S ;
BARLOGIE, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (09) :602-605
[6]   MULTICENTRIC CASTLEMANS DISEASE ASSOCIATED WITH RHEUMATOID-ARTHRITIS - A POSSIBLE ROLE OF HEPATITIS-B ANTIGEN [J].
BENCHETRIT, E ;
FLUSSER, D ;
OKON, E ;
ACKERMAN, Z ;
RUBINOW, A .
ANNALS OF THE RHEUMATIC DISEASES, 1989, 48 (04) :326-330
[7]  
BIENTZ M, 1977, SEM HOP PARIS, V53, P667
[8]  
BITTER MA, 1985, CANCER, V56, P188, DOI 10.1002/1097-0142(19850701)56:1<188::AID-CNCR2820560132>3.0.CO
[9]  
2-Z
[10]   DYSREGULATED INTERLEUKIN-6 EXPRESSION PRODUCES A SYNDROME RESEMBLING CASTLEMANS DISEASE IN MICE [J].
BRANDT, SJ ;
BODINE, DM ;
DUNBAR, CE ;
NIENHUIS, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (02) :592-599