Therapeutic plasma exchange as a bridge to definitive treatment in severe thyrotoxicosis with propylthiouracil-induced neutropenia [0.03%]
丙硫氧嘧啶所致中性粒细胞减少严重甲状腺毒症的治疗性血浆置换术作为最终治疗手段的过渡疗法
Sanja Medenica,Vladimir Prelević,Filip Tomovic et al.
Sanja Medenica et al.
Summary: A 67-year-old Caucasian woman with a history of Graves' disease and atrial fibrillation presented with severe symptoms indicative of an impending thyroid storm, including diarrhea, tremors, palpitations and signi...
Necrolytic migratory erythema following prolonged continuous subcutaneous dasiglucagon administration: a rare dermatologic adverse event [0.03%]
长期持续皮下注射索格鲁卡尼后的罕见皮肤不良反应——脱屑性迁徙红斑
Lucas Weschle,Jenny Potratz,Frank Rutsch et al.
Lucas Weschle et al.
Summary: Clinical management of congenital hyperinsulinism (CHI) remains a significant challenge due to its complex pathophysiology and the limitations of available therapies. Dasiglucagon, a synthetic glucagon analog, re...
Sequential development of hyperinsulinemic hypoglycemia and type 1 diabetes mellitus in a male child with trisomy 13 [0.03%]
一个13三体综合症男性儿童出现1型糖尿病和高胰岛素血症的发病过程研究
Satoru Sugimoto,Hidechika Morimoto,Tatsuji Hasegawa et al.
Satoru Sugimoto et al.
Summary: We present a rare case of a 19-month-old boy with trisomy 13 who initially presented with hyperinsulinemic hypoglycemia (HH) at 1 month of age and later developed type 1 diabetes mellitus (T1DM). While cases of H...
Adrenocortical carcinoma classified as benign: the limitations of washout values [0.03%]
washout值的局限性：一种被诊断为良性的肾上腺皮质癌病例报告
P S Yap,S Philip,A J Graveling et al.
P S Yap et al.
Summary: The new European Society of Endocrinology guidelines on the management of adrenal incidentalomas suggest discussion in a multidisciplinary meeting and consideration of additional imaging for homogenous lesions wi...
Multi-disciplinary collaboration in diagnosing thymic hyperplasia in a Graves' disease patient [0.03%]
多学科合作在Graves病伴胸腺生理性增生中的应用
Khin Yadanar Kyaw,Min Thant Lwin,Alistair Gummow et al.
Khin Yadanar Kyaw et al.
Summary: Thymic hyperplasia in Graves' disease is rarely identified due to the absence of routine imaging, but not uncommonly present. It is usually seen when imaging is performed for other reasons. Despite thymic hyperpl...
Horner's syndrome after an ultrasound-guided fine-needle aspiration puncture of a thyroid nodule [0.03%]
超声引导下甲状腺结节细针穿刺后霍纳综合征的發生
Alexandra Abegão Matias,Teresa Sabino,José Silva-Nunes
Alexandra Abegão Matias
Summary: Horner's syndrome is a rare condition that results from damage to the oculosympathetic chain. The classical presentation consists of miosis, unilateral ptosis and hemifacial anhidrosis due to a deficiency of symp...
Precocious puberty in male with hypertension and hypokalemia; a definite diagnostic clue for 11β hydroxylase deficiency CAH [0.03%]
高血压低血钾男性患儿早现青春发育征象，21-羟化酶不足的同型胱氨酸尿症的确诊线索
Minal Pande,Shinjan Patra,Kishore K Katam et al.
Minal Pande et al.
Summary: 11β-hydroxylase deficiency (11βOHD) (5-7%) is an uncommon cause of congenital adrenal hyperplasia compared to 21-hydroxylase deficiency (21OHD) (90%). We report a case of a 5-year-old boy who presented with gon...
Luke Vroegindewey,John Kim,Dennis J Joseph
Luke Vroegindewey
Summary: Papillary thyroid carcinoma (PTC) in a branchial cleft cyst (BCC) is exceedingly rare. This case report describes a 53-year-old male with a BCC containing PTC. Despite normal preoperative thyroid imaging, total t...
Accuracy validation and user performance analysis of two new self-monitoring blood glucose systems [0.03%]
两种新的血糖自我监测系统的准确性验证和用户性能分析
Tun-Yu Huang,Yu-Hsi Chen,Yu-Ching Li et al.
Tun-Yu Huang et al.
Summary: Patients with diabetes require regular blood glucose monitoring. We evaluated the precision and user performance of two blood glucose monitoring systems, the accuracy results of GlucoTeq BGM200 and DiaRite BGM300...
Resistant hypertension post-transsphenoidal surgery for pituitary Cushing's disease, leading to a diagnosis of primary aldosteronism [0.03%]
经蝶手术治疗垂体库欣病后出现的难治性高血压最终诊断为原发性醛固酮增多症
Jack Lee,Maria Tomkins,Darran McDonald et al.
Jack Lee et al.
Summary: We describe a case of a 42-year-old gentleman, 5 years post-transsphenoidal surgery (TSS) for pituitary-dependent Cushing's disease, initially presenting with malignant hypertension. Despite an initial improvemen...