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在获得性特发性全身性无汗症患者中,始终会出现与外分泌腺碳酸酐酶II表达降低相关的透明细胞损伤。

Clear cell injury associated with reduced expression of carbonic anhydrase II in eccrine glands consistently occurs in patients with acquired idiopathic generalized anhidrosis.

作者信息

Sano Kenji, Asahina Masato, Uehara Takeshi, Araki Nobuyuki, Yamanaka Yoshitaka, Matsumoto Kazuhiko, Okuyama Ryuhei

机构信息

Department of Pathology, Iida Municipal Hospital, Nagano, Japan.

Department of Laboratory Medicine, Shinshu University Hospital, Nagano, Japan.

出版信息

J Dermatol. 2021 Apr;48(4):439-446. doi: 10.1111/1346-8138.15722. Epub 2021 Jan 16.

Abstract

Acquired idiopathic generalized anhidrosis (AIGA) is characterized by anhidrosis/hypohidrosis without other autonomic and neurological dysfunctions. It has been believed that AIGA patients usually present no significant morphological alterations in the secretory portion of eccrine glands consisting of clear, dark and myoepithelial cells. However, we have recently revealed morphological damage of eccrine glands in AIGA patients by immunohistochemistry. Moreover, inhibitory side-effects against carbonic anhydrase II (CA II) by the antiepileptic reagent topiramate have been reported to cause heat intolerance mimicking AIGA. To determine the precise morphological changes and CA II expression in eccrine glands of AIGA patients, electron microscopic observation and immunohistochemistry were applied to skin of both anhidrotic (non-sweating) and normohidrotic (sweating-preserved) sites, taken from each patient clinically diagnosed with AIGA. We found consistent clear cell injury in eccrine glands in anhidrotic skin samples of AIGA patients. Electron micrographs demonstrated edematous, swollen and destructive damage in clear cells of eccrine glands from non-sweating areas of almost all AIGA patients. Immunohistochemically, clear cells showed reduced CA II expression that was heterogeneously distributed in non-sweating skin. Some areas showed almost complete loss of CA II expression in spite of preserved dark cells, and others showed mild or moderate loss of it. Selective destruction of clear cells resulting in heterogenous atrophy in AIGA patients may be important to elucidate its etiology.

摘要

获得性特发性全身性无汗症(AIGA)的特征是无汗/少汗,且无其他自主神经和神经功能障碍。人们一直认为,AIGA患者由透明细胞、暗细胞和肌上皮细胞组成的小汗腺分泌部通常没有明显的形态学改变。然而,我们最近通过免疫组织化学揭示了AIGA患者小汗腺的形态学损伤。此外,据报道,抗癫痫药物托吡酯对碳酸酐酶II(CA II)的抑制性副作用会导致类似AIGA的耐热性降低。为了确定AIGA患者小汗腺的确切形态变化和CA II表达情况,我们对临床诊断为AIGA的每位患者无汗(不出汗)和正常出汗部位的皮肤进行了电子显微镜观察和免疫组织化学检测。我们发现AIGA患者无汗皮肤样本中的小汗腺存在一致的透明细胞损伤。电子显微镜照片显示,几乎所有AIGA患者不出汗区域的小汗腺透明细胞出现水肿、肿胀和破坏性损伤。免疫组织化学检测显示,透明细胞中CA II表达减少,在不出汗皮肤中呈异质性分布。尽管暗细胞保存完好,但有些区域CA II表达几乎完全丧失,而其他区域则表现为轻度或中度丧失。AIGA患者中透明细胞的选择性破坏导致异质性萎缩,这可能对阐明其病因很重要。

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