生长激素缺乏和继发性肾上腺功能不全伴石化耳综合征1例报告并文献复习。

IF 1.3 Q2 DERMATOLOGY
Dermatology Reports Pub Date : 2025-08-22 Epub Date: 2025-01-31 DOI:10.4081/dr.2025.10263
Sebastiano Recalcati, Alberto Vassallo, Marta Villanova, Roberto Lanzi, Marco Losa, Maria Grazia Patricelli, Paola Carrera, Fabrizio Fantini
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引用次数: 0

摘要

石化耳是一种罕见的临床实体,其特征是正常的柔性耳廓软骨进行性硬化,导致部分或完全耳廓僵硬。在许多情况下,它提供了有价值的临床线索,使临床医生能够在未得到诊断的患者中发现内分泌病变(特别是Addison病)。我们提出了第一个记录的石化耳病例,导致继发性肾上腺素减退和生长激素缺乏症(GHD)的诊断。此外,我们回顾了相关文献。石化耳综合征可能是其他全身性疾病的一种被低估的临床表现。有时,即使在没有典型特征的情况下,它也可以作为怀疑潜在内分泌疾病的有用而简单的临床线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Growth hormone deficiency and secondary adrenal insufficiency in petrified ear syndrome: a case report and literature review.

Growth hormone deficiency and secondary adrenal insufficiency in petrified ear syndrome: a case report and literature review.

Growth hormone deficiency and secondary adrenal insufficiency in petrified ear syndrome: a case report and literature review.

Growth hormone deficiency and secondary adrenal insufficiency in petrified ear syndrome: a case report and literature review.

Petrified ear is a rare clinical entity characterized by the progressive hardening of normal, flexible auricular cartilage, leading to partial or complete auricular stiffness. In many cases, it provides a valuable clinical clue that allows the clinician to detect endocrinopathies (particularly Addison's disease) in a patient who has not received a diagnosis. We present the first documented case of petrified ears, which resulted in the diagnosis of both secondary hypoadrenalism and growth hormone deficiency (GHD). Additionally, we review the relevant literature. Petrified ear syndrome is probably an underreported clinical manifestation of other systemic disorders. It may, at times, serve as a valuable and simple clinical clue to suspect underlying endocrinopathies even in the absence of typical features.

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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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