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儿童皮下环状肉芽肿:34例临床病理特征

Subcutaneous granuloma annulare in childhood: clinicopathologic features in 34 cases.

作者信息

Grogg K L, Nascimento A G

机构信息

Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

Pediatrics. 2001 Mar;107(3):E42. doi: 10.1542/peds.107.3.e42.

Abstract

OBJECTIVE

To gather clinicopathologic data on subcutaneous granuloma annulare (SGA), a subtype of granuloma annulare that occurs exclusively in children and is histologically similar to rheumatoid nodules.

DESIGN

Retrospective record review.

PATIENTS

Children <10 years old in whom SGA, deep granuloma annulare, or necrobiotic granuloma was diagnosed at the Mayo Clinic (Rochester, MN) from 1983 to 1998.

RESULTS

Thirty-four patients (21 girls and 13 boys; average age at diagnosis: 4.6 years) were found to have SGA. The lesions predominantly occurred in the lower extremity, especially in a pretibial location. Local recurrence within 1 month to 7 years was documented in 38.2%; recurrence at other locations was documented in 14.7%. Average follow-up was 60 months; during follow-up, no patients developed signs or symptoms of rheumatologic disease. Insulin-dependent diabetes mellitus was diagnosed in 2 patients, 1 before the development of SGA and 1 after it by 1 month.

CONCLUSIONS

SGA is a lesion that presents as subcutaneous nodules on the lower extremities, hands, or scalp in young children. Recurrence is common but usually does not warrant additional biopsy.

摘要

目的

收集有关皮下环状肉芽肿(SGA)的临床病理数据,SGA是环状肉芽肿的一种亚型,仅发生于儿童,组织学上与类风湿结节相似。

设计

回顾性病历审查。

患者

1983年至1998年在梅奥诊所(明尼苏达州罗切斯特)被诊断为SGA、深部环状肉芽肿或渐进性坏死性肉芽肿的10岁以下儿童。

结果

发现34例患者(21名女孩和13名男孩;诊断时平均年龄:4.6岁)患有SGA。病变主要发生在下肢,尤其是胫前部位。1个月至7年内局部复发率为38.2%;其他部位复发率为14.7%。平均随访60个月;随访期间,无患者出现风湿性疾病的体征或症状。2例患者被诊断为胰岛素依赖型糖尿病,1例在SGA出现之前,1例在SGA出现后1个月。

结论

SGA是一种在幼儿下肢、手部或头皮上表现为皮下结节的病变。复发很常见,但通常无需再次活检。

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