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原发性甲状腺功能减退症表现为假性肢端肥大症。

Primary hypothyroidism presenting as pseudoacromegaly.

机构信息

Department of Endocrinology, Command Hospital, Lucknow, UP, 226002, India.

出版信息

Pituitary. 2012 Dec;15 Suppl 1:S49-52. doi: 10.1007/s11102-011-0336-x.

DOI:10.1007/s11102-011-0336-x
PMID:21805092
Abstract

Pseudoacromegaly is a condition characterized by cutaneous manifestations of growth hormone excess but with normal growth hormone levels. This is described in patients with severe insulin resistance, pachydermoperiostitis, burnt out acromegaly and with intake of drugs like Minoxidil. Severe thyroid hormone deficiency rarely present with similar picture and the issue is further complicated in presence of pituitary hyperplasia. We report an unusual presentation of primary hypothyroidism with pseudoacromegaly and thyrotroph hyperplasia mimicking a pituitary macroadenoma. The thyrotroph hyperplasia resolved completely with levothyroxine therapy.

摘要

假性肢端肥大症是一种以生长激素过多的皮肤表现为特征,但生长激素水平正常的疾病。这种疾病发生在严重胰岛素抵抗、厚皮性骨膜病、消耗性肢端肥大症和服用米诺地尔等药物的患者中。严重的甲状腺激素缺乏症很少出现类似的表现,而在存在垂体增生的情况下,问题会更加复杂。我们报告了一例原发性甲状腺功能减退症伴假性肢端肥大症和促甲状腺激素细胞增生的罕见表现,这种增生类似于垂体大腺瘤。促甲状腺激素细胞增生在用左甲状腺素治疗后完全消退。

相似文献

1
Primary hypothyroidism presenting as pseudoacromegaly.原发性甲状腺功能减退症表现为假性肢端肥大症。
Pituitary. 2012 Dec;15 Suppl 1:S49-52. doi: 10.1007/s11102-011-0336-x.
2
Pseudoacromegaly.假性肢端肥大症。
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Pituitary hyperplasia mimicking pituitary macroadenoma in two adolescent patients with long-standing primary hypothyroidism: case reports and review of literature.两名长期原发性甲状腺功能减退青少年患者中类似垂体大腺瘤的垂体增生:病例报告及文献复习
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Pituitary thyrotroph hyperplasia mimicking prolactin-secreting adenoma.酷似催乳素分泌腺瘤的垂体促甲状腺激素细胞增生
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Insulin resistance and pseudoacromegaly: A case report.胰岛素抵抗与假性肢端肥大症:一例报告
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引用本文的文献

1
Pituitary Hyperplasia Due to Longstanding Primary Hypothyroidism: A Case Report and Comprehensive Review of the Literature.长期原发性甲状腺功能减退所致垂体增生:1例报告及文献综述
Biomedicines. 2024 Jun 19;12(6):1368. doi: 10.3390/biomedicines12061368.
2
The Importance of Acromegaloid Physical Features for Clinical Practice.肢端肥大样身体特征在临床实践中的重要性。
Case Rep Endocrinol. 2023 Nov 18;2023:5583344. doi: 10.1155/2023/5583344. eCollection 2023.
3
Pituitary Hyperplasia in Severe Primary Hypothyroidism: A Case Report and Review of the Literature.

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