Bao Shunzhong S, Rapp Richard
Little Rock Diagnostic Clinic, Little Rock, Arkansas.
Endocr Pract. 2014 Mar;20(3):e42-6. doi: 10.4158/EP13116.CR.
To demonstrate that xanthogranuloma is a rare cause of idiopathic central diabetes insipidus in the early phase of the disease and that it presents as a suprasellar mass at a later stage. In addition, we emphasize the importance of identifying the cause of idiopathic central diabetes insipidus and review the literature concerning endocrine disturbance in central xanthogranuloma.
Review of recently published case reports of central xanthogranuloma with endocrine disorders. The case of a 35-year-old man who presented with a very large suprasellar mass is also reported. The patient was diagnosed with idiopathic central diabetes insipidus 20 years ago with normal brain magnetic resonance imaging.
Most cases of this disease present as supra- or parasellar masses with endocrine involvement, the most common of which (in approximately 75% of patients) is sex hormone deficiency. Diabetes insipidus was found in 65% of patients.
Xanthogranuloma should be in the differential diagnosis of idiopathic central diabetes insipidus and sellar and parasellar masses. A detailed skin examination is very important in making the diagnosis of central diabetes insipidus.
证明黄色肉芽肿是特发性中枢性尿崩症疾病早期的罕见病因,且在疾病后期表现为鞍上肿块。此外,我们强调明确特发性中枢性尿崩症病因的重要性,并回顾有关中枢性黄色肉芽肿内分泌紊乱的文献。
回顾近期发表的伴有内分泌紊乱的中枢性黄色肉芽肿病例报告。还报告了一名35岁男性患者的病例,该患者表现为巨大鞍上肿块。该患者20年前被诊断为特发性中枢性尿崩症,当时脑磁共振成像正常。
该疾病的大多数病例表现为伴有内分泌受累的鞍上或鞍旁肿块,其中最常见的(约75%的患者)是性激素缺乏。65%的患者出现尿崩症。
黄色肉芽肿应列入特发性中枢性尿崩症以及鞍区和鞍旁肿块的鉴别诊断中。详细的皮肤检查对中枢性尿崩症的诊断非常重要。