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肠系膜局限性Castleman病伴发三叉神经病变1例

Trigeminal neuropathy in a case of mesenteric localized Castleman's disease.

作者信息

Gabrielli G B, Bonetti F, Tognella P, Corrocher R, De Sandre G

机构信息

Istituto di Clinica Medica, Università di Verona, Italy.

出版信息

Haematologica. 1991 May-Jun;76(3):245-7.

PMID:1743597
Abstract

Peripheral neuropathy of the limbs has so far been observed in very few patients with localized Castleman's disease, generally of the plasma-cell type. In the present case report, of a plasmacellular type localized within the mesenterium, a 25-year-old woman exhibited a clinical picture of right trigeminal neuropathy (together with more common constitutional symptoms and laboratory findings), which promptly disappeared after surgical removal of the mesenteric mass. To our knowledge, a similar impairment of cranial nerves, and specifically of the trigeminal, has never been reported in patients with the localized form of Castleman's disease.

摘要

迄今为止,在极少数局限性Castleman病患者(通常为浆细胞型)中观察到肢体周围神经病变。在本病例报告中,一名25岁女性患有位于肠系膜内的浆细胞型局限性Castleman病,表现出右侧三叉神经病变的临床症状(伴有更常见的全身症状和实验室检查结果),在手术切除肠系膜肿块后症状迅速消失。据我们所知,局限性Castleman病患者从未有过类似的颅神经损害,尤其是三叉神经损害的报道。

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