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锌缺乏综合征与胰高血糖素瘤综合征

Zinc deficiency syndrome versus glucagonoma syndrome.

作者信息

Hoitsma H F, Cuesta M A, Starink T M, Uttendorfsky-van der Putten H J, van der Veen E A

出版信息

Arch Chir Neerl. 1979;31(3):131-40.

PMID:534435
Abstract

In this paper two patients with uncommon syndromes, viz. acrodermatitis enteropathica-like eruption due to acute zinc deficiency, when on long-term intravenous hyperalimentation for Crohn's disease, and necrolytic migratory erythema as a consequence of a malignant glucagon secreting alpha-cell tumour of the pancreas (glucagonoma syndrome) are reported. Attention is paid to the many common features of the skin lesions in both syndromes. This is discussed in detail. Both patients passed through a catabolic stage. Laboratory investigations, however, failed to demonstrate a common biochemical mechanism which might be responsible for the skin lesions. Administration of zinc in the first patient and surgical treatment of the second patient results in rapid clearing of the skin lesions and other symptoms.

摘要

本文报道了两名患有罕见综合征的患者,即一名因克罗恩病接受长期静脉高营养治疗而出现急性锌缺乏所致的肠病性肢端皮炎样皮疹患者,以及另一名因胰腺分泌胰高血糖素的恶性α细胞瘤(胰高血糖素瘤综合征)而出现坏死松解性游走性红斑的患者。文中关注了这两种综合征皮肤损害的诸多共同特征,并对此进行了详细讨论。两名患者均经历了分解代谢阶段。然而,实验室检查未能证实可能导致皮肤损害的共同生化机制。对第一名患者给予锌治疗,对第二名患者进行手术治疗后,皮肤损害及其他症状迅速消退。

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