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期刊名:Oxford medical case reports

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ISSN:2053-8855

e-ISSN:2053-8855

IF/分区:0.4/Q3

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共收录本刊相关文章索引1732
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Niels Nordin,Mamoun Ahmed,Frederik Boxberg et al. Niels Nordin et al.
Ventriculoperitoneal (VP) shunt migration and anal protrusion is a very rare complication of VP Shunt Implantation, which is more often seen in children then adults. We present a case of a 72-year-old female with severe diverticulosis and a...
Hironori Ando,Yayoi Kuwabara-Ohmura,Akira Sumida et al. Hironori Ando et al.
Needle tract seeding (NTS) is a rare complication of fine-needle aspiration cytology (FNAC). An 87-year-old man presented with a subcutaneous cervical nodule. Eighteen years prior, he had undergone right thyroid lobectomy owing to tracheal ...
Mohammed Albahloul Rajab,Abdalla Mohamed Hamed,Riad Elmabrouk Esloughi et al. Mohammed Albahloul Rajab et al.
Hepatitis A is typically a self-limiting viral infection of the liver. Patients with hepatitis A may exhibit a wide range of clinical manifestations, from asymptomatic infection to fulminant liver failure. However, extra-hepatic manifestati...
Salma Barakat,Rayan Yousif,Ahmed Rafei et al. Salma Barakat et al.
Gastric carcinoids (GCDs) are rare neuroendocrine tumors that can occasionally present with upper gastrointestinal bleeding. We report a case of a 60-year-old male who presented with hematemesis due to a gastric carcinoid tumor. Emergency g...
Farah Ibraik,Ibraheem Hammouri,Hasan Arafat et al. Farah Ibraik et al.
Silver-Russell syndrome (SRS), also known as Russell-Silver syndrome (RSS), is a congenital growth disorder characterized by intrauterine and postnatal growth retardation, craniofacial disproportion, asymmetry, and other distinctive feature...
Sulymon A Saka Sulymon A Saka
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rare autosomal recessive disorder marked by cortisol deficiency, it often presents with adrenal crises and ambiguous genitalia in 46, XX neonates. Isolated cleft pal...
Poorva Vias,Ashish Saklani,Mayur Garkar et al. Poorva Vias et al.
Choroidal metastasis is a rare but significant manifestation of systemic malignancies, most commonly originating from breast and lung cancers. Metastatic spread to the choroid from colorectal cancer (CRC) is exceedingly uncommon, with limit...
Yoshikazu Mutoh,Tomonori Sato,Yuko Oya et al. Yoshikazu Mutoh et al.
A 69-year-old man followed post lung cancer surgery for 6 years presented with back pain. His imaging revealed a pleural abscess and rib osteomyelitis along with the surgical site. Therefore, bone biopsy and culture were performed and the o...
Georgina Hadfield,Mark Harrison Georgina Hadfield
Acute Flaccid paralysis is a rare presentation of severe hyperkalaemia, described rarely in the literature. We report a case of flaccid paralysis, including cranial nerve involvement, secondary to hyperkalaemia in a patient presenting to A&...
Vinson James,Yonique Petgrave Vinson James
Background: Thymoma, commonly seen in middle-aged and elderly individuals, is associated with autoimmune disorders. While renal involvement is rare, its occurrence remains poorly characterized. ...