Florid reactive follicular hyperplasia in elderly patients. A clinicopathological study of 23 cases

被引:10
作者
Kojima, M
Nakamura, S
Shimizu, K
Itoh, H
Yoshida, K
Hosomura, Y
Yamane, N
Ban, S
Joshita, T
Suchi, T
机构
[1] Ashikaga Red Cross Hosp, Dept Pathol, Ashikaga, Tochigi 3260808, Japan
[2] Ashikaga Red Cross Hosp, Clin Labs, Ashikaga, Tochigi 3260808, Japan
[3] Aichi Canc Ctr Hosp, Dept Pathol, Nagoya, Aichi 464, Japan
[4] Ashikaga Red Cross Hosp, Clin Labs, Ashikaga, Tochigi 3260808, Japan
[5] Natl Tochigi Hosp, Dept Pathol, Utsunomiya, Tochigi, Japan
[6] Natl Tochigi Hosp, Clin Labs, Utsunomiya, Tochigi, Japan
[7] Maebashi Red Cross Hosp, Dept Pathol, Maebashi, Gumma, Japan
[8] Maebashi Red Cross Hosp, Clin Labs, Maebashi, Gumma, Japan
[9] Kiryu Welf Gen Hosp, Dept Pathol, Kiryu, Gumma, Japan
[10] Kiryu Welf Gen Hosp, Clin Labs, Kiryu, Gumma, Japan
[11] Sano Welf Gen Hosp, Dept Pathol, Sano, Japan
[12] Sano Welf Gen Hosp, Clin Labs, Sano, Japan
[13] Gunma Univ, Sch Med, Dept Clin Labs, Maebashi, Gumma 371, Japan
关键词
reactive follicular hyperplasia; elderly patients; autoimmune disease; plasma cells; Castleman's disease;
D O I
10.1016/S0344-0338(98)80029-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Florid reactive follicular hyperplasia (FRFH) of the enlarged lymph node in elderly patients requiring biopsy is a relatively uncommon phenomenon as compared with younger age groups. We experienced 23 patients, aged 60 years or more, from whom the biopsied lymph node specimens histologically showed inappropriate FRFH for their age, in the period between 1982 and 1996. These cases were morphologically subdivided into three groups, FRFH with interfollicular plasmacy tosis, that with progressive transformation of germinal center, and FRFH without additional specific findings. FRFH with interfollicular plasmacytosis were observed in 11 cases, all of whom were accompanied with several immunological abnormalities (six with rheumatoid arthritis, three with multicentric Castleman's disease and one each with myoepithelial sialoadenitis and autoimmune hemolytic anemia). Three men with uncertain etiology exhibited an unusual histology of progressive transformed germinal centers which were clinically characterized by a bulky neck mass. Among the nine cases with nonspecific FRFH, only four had a specific etiology tone each with adult onset Still's disease, chronic sinusitis, Epstein-Barr virus infection and infectious lateral cervical cyst), while the other five with unknown etiology showed abnormal laboratory findings suggestive of an abnormal humoral immune response, i.e, hypergammaglobulinemia and seropositivities for some autoantibodies. None of our patients developed malignant lymphoma during the follow-up period. Of note, 16 (70%) of the 23 cases were found to be associated with various types of imbalances of the immune system, some of which appeared to be currently ill-defined as clinicopathological entities that were simply categorized as autoimmune disease.
引用
收藏
页码:391 / 397
页数:7
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