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股骨头骨骺滑脱症与垂体大腺瘤所致全垂体功能减退症的相关性:病例报告。

Association of Slipped Capital Femoral Epiphysis With Panhypopituitarism Due to Pituitary Macroadenoma: A Case Report.

机构信息

University of Alabama at Birmingham, AL, USA.

Andrews Sports Medicine & Orthopaedic Center, Birmingham, AL, USA.

出版信息

J Investig Med High Impact Case Rep. 2021 Jan-Dec;9:2324709621999956. doi: 10.1177/2324709621999956.

Abstract

Slipped capital femoral epiphysis (SCFE) commonly occurs in overweight or obese adolescents, but can also be associated with endocrine disorders including hypothyroidism, pituitary tumors, and growth hormone deficiency. In this article, we present a case of panhypopituitarism that initially presented with SCFE. A 16-year-old male presented with right SCFE. After a right hip open reduction and percutaneous pinning procedure, findings of skeletal maturity that lagged behind his chronologic age and a delayed Tanner stage resulted in a referral to an endocrine specialist. Endocrine laboratory evaluation identified elevated prolactin levels (1493 ng/mL), hypogonadotropic hypogonadism, and central adrenal insufficiency as evidenced by low morning cortisol level of 1.0 µg/dL. Magnetic resonance imaging revealed a large pituitary T2 isointense mass measuring 1.8 × 2.7 × 2.3 cm. The patient was diagnosed with panhypopituitarism due to a pituitary macroadenoma. Multidisciplinary collaboration for treatment of this patient consisted of oral cabergoline, oral levothyroxine, oral hydrocortisone therapy, intramuscular testosterone therapy, and a prophylactic closed reduction percutaneous pinning of the left hip due to high risk of also developing SCFE of the left hip. Panhypopituitarism should be considered as a diagnosis after atypical presentations of SCFE. In our case, an astute clinical assessment resulted in prompt endocrine referral and management of panhypopituitarism. Our report highlights the importance of multidisciplinary collaborations to guarantee early detection of endocrinopathies in patients with SCFE undergoing surgical interventions in order to avoid potential complications, such as adrenal crisis during surgery.

摘要

股骨头骨骺滑脱(SCFE)通常发生于超重或肥胖的青少年中,但也可能与内分泌紊乱有关,包括甲状腺功能减退、垂体肿瘤和生长激素缺乏症。本文报告了 1 例以 SCFE 起病的全垂体功能减退症。16 岁男性,右侧 SCFE。右侧髋关节切开复位和经皮钢针固定术后,发现骨骼成熟度落后于其实际年龄,且 Tanner 分期延迟,故转诊至内分泌科专家。内分泌实验室检查发现催乳素水平升高(1493ng/ml)、促性腺激素低下性性腺功能减退症和中枢性肾上腺功能不全,表现为清晨皮质醇水平低至 1.0µg/dL。磁共振成像显示一个大的垂体 T2 等信号肿块,大小为 1.8×2.7×2.3cm。患者被诊断为垂体大腺瘤所致全垂体功能减退症。该患者的治疗涉及多学科合作,包括口服卡麦角林、左甲状腺素钠、口服氢化可的松治疗、肌肉注射睾酮治疗,以及预防性闭合复位经皮钢针固定左侧髋关节,因为左侧髋关节也有发生 SCFE 的高风险。在 SCFE 不典型表现后,应考虑全垂体功能减退症作为诊断。在我们的病例中,敏锐的临床评估导致及时进行内分泌转诊和全垂体功能减退症的管理。我们的报告强调了多学科合作的重要性,以保证在接受手术干预的 SCFE 患者中早期发现内分泌疾病,以避免潜在的并发症,如手术期间的肾上腺危象。

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