Amin Khan,Aditya Duhan,Rajiv Mangla et al.
Amin Khan et al.
Hirayama disease (HD) is a rare cervical myelopathy involving lower cervical myotomes, causing asymmetric or unilateral distal upper extremity muscle atrophy. Diagnosis relies on clinical findings, nerve conduction studies, and cervical spi...
G-CSF-induced Aortitis in an elderly woman successfully managed with prednisolone: a case report and literature review [0.03%]
一项老年女性粒细胞集落刺激因子诱导的主动脉炎成功采用泼尼松龙治疗个例及其文献综述
Taeko Kurosawa,Masahiro Ohara,Ayako Nakame et al.
Taeko Kurosawa et al.
Cancer incidence among old is increasing. Since age is important risk factor for febrile neutropenia (FN), use of granulocyte-colony stimulating factor (G-CSF) and its complication is clinically important. A 72-year old woman has completed ...
An unusual presentation of cutaneous sarcoidosis induced by Koebner's phenomenon [0.03%]
科布纳现象所致皮肤结节病一例报告
Maryam Ghaleb,Ouiame El Jouari,Salim Gallouj
Maryam Ghaleb
We report an unusual case of cutaneous sarcoidosis presenting as papulonodular lesions strictly localized to the nasal bridge and medial canthus-corresponding to areas of pressure from eyeglass frames. This rare distribution suggests the in...
Precocious puberty in a rural Guatemalan boy: Unraveling the role of malnutrition and psychosocial stress [0.03%]
危地马拉农村一男孩早熟病例报告：营养不良与心理社会压力的致病作用分析
Andrea Argueta,Q Carlos Diaz,Victor Hugo Argueta et al.
Andrea Argueta et al.
Precocious puberty is a rare condition, particularly in boys, characterized by the early development of secondary sexual characteristics. This case report presents a 5-year-old male from rural Guatemala who exhibited signs of accelerated se...
Pollakiuria: a rare and unique mode of revelation of silent dorsal syringomyelia in a young man-a case report [0.03%]
多尿：年轻男性隐性背侧脊髓空洞症的罕见且独特的表现形式-病例报告
Richard Houeze,Mendinatou Agbetou Houessou,Alexandre D Faton et al.
Richard Houeze et al.
Introduction: Syringomyelia is a rare pathology which is rarely revealed by urinary urgency. We report the case of a 20-year-old man with persistent urinary urgency and pollakiuria for two years, with no identifiable orga...
Pediatric Sneddon syndrome presenting with early-onset liver fibrosis: a rare case report [0.03%]
儿童Sneddon综合征合并早期肝纤维化1例报告
Qutaiba N Awad,Taha Z Makhlouf,Mohammad F Zhour et al.
Qutaiba N Awad et al.
Sneddon syndrome (SS) is a rare neurocutaneous disorder consisting of livedo racemosa (LR) and cerebrovascular disease with an incidence of 4 per 1 000 000 annually. It may be idiopathic or associated with autoimmune or genetic factors, inc...
Immune thrombocytopenia as a rare initial manifestation and complication of Hodgkin lymphoma: a Pediatric case report [0.03%]
霍奇金淋巴瘤的罕见初始表现和并发症——免疫性血小板减少症：一例儿科病例报告
Mohammad Obada Alsadi,Mohammed Swileh,Fatmah Alshiajy et al.
Mohammad Obada Alsadi et al.
Hodgkin lymphoma (HL) is a malignancy of the lymphatic system often associated with immune dysfunction. This case describes an 11-year-old boy presenting with epistaxis, petechiae, and thrombocytopenia (40 000/μl), initially diagnosed as i...
Hemorrhagic brain metastasis as the initial presentation of osteosarcoma: a rare case report [0.03%]
骨肉瘤首次表现为出血性脑转移一例罕见病例报道
Salma El Aouadi,Rania Bouanane,Soukaina Bahha et al.
Salma El Aouadi et al.
Osteosarcoma is the most common malignant bone tumor in children and adolescents, with a predilection for long bones and frequent pulmonary metastases. Brain metastases are rare, occurring in 1.8% to 5.6% of cases, and hemorrhagic ones are ...
A rare etiology of right lower back pain in a young man: contained rupture of the common iliac artery aneurysm [0.03%]
年轻男性右下背痛的罕见病因：髂总动脉瘤含囊破裂
Ouiam Taibi,Rania Bouanane,Salma Elaouadi et al.
Ouiam Taibi et al.
Relatively rare aneurysms of the common iliac artery are abnormal dilatations of the vessel, which can be complicated by a rupture that, in rarer cases, may be contained by surrounding structures. Imaging, particularly CT angiography, plays...
Rova Malala Fandresena Randrianarisoa,Mathilde Tonnelier,Morgane Mailhe et al.
Rova Malala Fandresena Randrianarisoa et al.
Introduction: Infective endocarditis is a rare complication of untreated Whipple's disease. We present a case of infective endocarditis caused by Tropheryma whipplei in an aortic bioprosthesis. ...