Oxford Medical Case Reports最新文献_第4页

Lupus vulgaris with a pseudo tumoral presentation, case report. 假性肿瘤表现的寻常性狼疮1例。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-09-15 eCollection Date: 2025-09-01 DOI: 10.1093/omcr/omaf154

Fatima Zohra El Ali, Salim Gallouj, Kaoutar Benchakroune, Imane Talhaoui, Ouiame El Jouari

引用次数: 0

G-CSF-induced Aortitis in an elderly woman successfully managed with prednisolone: a case report and literature review. 强的松龙成功治疗老年妇女g - csf诱导的主动脉炎：1例报告和文献复习。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf144

Taeko Kurosawa, Masahiro Ohara, Ayako Nakame, Yuki Ichinose, Akihiro Fujimoto, Asami Nukui, Kei Yamaguchi, Aya Asano, Hiroko Shimada, Hideki Yokogawa, Kazuo Matsuura, Hiroshi Ishiguro, Takahiro Hasebe, Akihiko Osaki, Toshiaki Saeki

{"title":"G-CSF-induced Aortitis in an elderly woman successfully managed with prednisolone: a case report and literature review.","authors":"Taeko Kurosawa, Masahiro Ohara, Ayako Nakame, Yuki Ichinose, Akihiro Fujimoto, Asami Nukui, Kei Yamaguchi, Aya Asano, Hiroko Shimada, Hideki Yokogawa, Kazuo Matsuura, Hiroshi Ishiguro, Takahiro Hasebe, Akihiko Osaki, Toshiaki Saeki","doi":"10.1093/omcr/omaf144","DOIUrl":"10.1093/omcr/omaf144","url":null,"abstract":"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 definitive surgery for left breast cancer and was started on postoperative chemotherapy. After 12 doses of paclitaxel, she received 1st cycle of epirubicin and cyclophosphamide (day 1), and pegfilgrastim, a pegylated G-CSF to decrease the risk of FN (day 2). On day 13, she was admitted due to persistent fever since day 9. Laboratory tests revealed elevated neutrophil counts and C-reactive protein. Despite empirical antibiotics, her fever persisted and severe back pain developed (day 15). Contrast-enhanced computed tomography revealed wall thickening and increased density around the aortic arch and brachiocephalic artery. Diagnosis of pegfilgrastim-induced vasculitis was made after excluding autoimmune vasculitis. Prednisolone (60 mg/day) was administered and the fever and back pain subsided the following day.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 8","pages":"omaf144"},"PeriodicalIF":0.4,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375805/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Precocious puberty in a rural Guatemalan boy: Unraveling the role of malnutrition and psychosocial stress. 危地马拉农村男孩的性早熟：揭示营养不良和社会心理压力的作用。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf150

Andrea Argueta, Q Carlos Diaz, Victor Hugo Argueta, Marian Vasquez

引用次数: 0

Pollakiuria: a rare and unique mode of revelation of silent dorsal syringomyelia in a young man-a case report. Pollakiuria：一种罕见而独特的方式揭示沉默背侧脊髓空洞在一个年轻人的病例报告。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf149

Richard Houeze, Mendinatou Agbetou Houessou, Alexandre D Faton, Salim Djaouga, Richmine Covi Zinsou, Eugénie Dansou, Martial Avoce, Constant K Adjien

{"title":"Pollakiuria: a rare and unique mode of revelation of silent dorsal syringomyelia in a young man-a case report.","authors":"Richard Houeze, Mendinatou Agbetou Houessou, Alexandre D Faton, Salim Djaouga, Richmine Covi Zinsou, Eugénie Dansou, Martial Avoce, Constant K Adjien","doi":"10.1093/omcr/omaf149","DOIUrl":"10.1093/omcr/omaf149","url":null,"abstract":"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 organic cause despite a thorough urological work-up. A transient episode of lower limb atony prompted spinal MRI, which revealed an isolated syrinx at the T6-T7 level, without associated Chiari malformation or conus medullaris involvement. The final diagnosis was vesico-sphincter dyssynergia with overactive bladder syndrome secondary to idiopathic thoracic syringomyelia. Conservative management, including anticholinergic therapy and psychological support, led to significant clinical improvement.Conclusion: As illustrated by our case, syringomyelia may present exclusively with urinary symptoms. However, such presentation is uncommon. This case highlights the importance of considering spinal cord pathology in the differential diagnosis of unexplained urinary symptoms, even in the absence of overt neurological deficits.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 8","pages":"omaf149"},"PeriodicalIF":0.4,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973521","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

An unusual presentation of cutaneous sarcoidosis induced by Koebner's phenomenon. 由Koebner现象引起的皮肤结节病的不寻常表现。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf147

Maryam Ghaleb, Ouiame El Jouari, Salim Gallouj

引用次数: 0

Isolated syndrome of inappropriate antidiuresis (SIAD) after Transphenoidal surgery of a non-functioning pituitary adenoma: clinical case report. 无功能垂体腺瘤经蝶窦手术后不适当抗利尿的孤立综合征：临床病例报告。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf152

Nasthia Quilismal, Mariana Risso, Patricia Agüero, Ramilo Lima, Francisco Garagorry, Dardo Centurion, Maria M Pineyro

{"title":"Isolated syndrome of inappropriate antidiuresis (SIAD) after Transphenoidal surgery of a non-functioning pituitary adenoma: clinical case report.","authors":"Nasthia Quilismal, Mariana Risso, Patricia Agüero, Ramilo Lima, Francisco Garagorry, Dardo Centurion, Maria M Pineyro","doi":"10.1093/omcr/omaf152","DOIUrl":"10.1093/omcr/omaf152","url":null,"abstract":"Introduction: Disorders of water balance, including arginine vasopressin deficiency (AVP-D) and syndrome of inappropriate antidiuresis (SIAD), are common postoperative complications following pituitary surgery. While AVP-D typically occurs as an isolated condition, SIAD may also present independently.Clinical case: We describe the case of a patient with a non-functioning pituitary adenoma who underwent transsphenoidal surgery. On postoperative day 7, she developed isolated SIAD, characterized by a plasma sodium level of 113 mmol/L, normovolemia, urine osmolality of 364 mOsm/kg, and urine sodium concentration of 50 mmol/L. A daily fluid restriction of 800 mL resulted in the resolution of hyponatremia within 48 h.Conclusions: Water balance disorders following pituitary surgery are often unpredictable. This case highlighs the importance of close postoperative clinical and biochemical monitoring. Vigilance is essential, even in the absence of AVP-D, to ensure early detection and management of potentially severe complications such as SIAD.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 8","pages":"omaf152"},"PeriodicalIF":0.4,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375806/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973467","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Pediatric Sneddon syndrome presenting with early-onset liver fibrosis: a rare case report. 儿童斯奈登综合征表现为早发性肝纤维化：罕见病例报告。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf153

Qutaiba N Awad, Taha Z Makhlouf, Mohammad F Zhour, Sami Bannoura, Wesam Abu Hussein

{"title":"Pediatric Sneddon syndrome presenting with early-onset liver fibrosis: a rare case report.","authors":"Qutaiba N Awad, Taha Z Makhlouf, Mohammad F Zhour, Sami Bannoura, Wesam Abu Hussein","doi":"10.1093/omcr/omaf153","DOIUrl":"10.1093/omcr/omaf153","url":null,"abstract":"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, including deficiency of adenosine deaminase 2 (DADA2). We describe a 17-month-old girl with recurrent fevers, hepatosplenomegaly, LR, and progressive liver fibrosis. A pathogenic ADA2 mutation and LDLR mutation associated with familial hypercholesterolemia (FH) were detected by genetic testing. Despite corticosteroids, etanercept, and immunosuppressants, she continued to deteriorate and developed portal vein thrombosis and increasing hepatic dysfunction. DADA2 is well described to cause systemic vasculopathy, but its association with liver fibrosis is still unclear. Our case highlights a potential association between DADA2 and LDLR mutation leading to hepatic injury, extending the broad spectrum of SS-related complications. Further research is needed to understand the role of these genes and their mutations in the systemic and hepatic manifestations of SS.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 8","pages":"omaf153"},"PeriodicalIF":0.4,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12375808/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973527","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Hirayama disease: a rare cause of cervical myelopathy. 平山病：颈椎病的罕见病因。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-25 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf151

Amin Khan, Aditya Duhan, Rajiv Mangla, Manisha Mangla, Sajjad Ghanim Al-Badri

引用次数: 0

Immune thrombocytopenia as a rare initial manifestation and complication of Hodgkin lymphoma: a Pediatric case report. 免疫性血小板减少症是霍奇金淋巴瘤罕见的初始表现和并发症：一个儿科病例报告。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-20 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf136

Mohammad Obada Alsadi, Mohammed Swileh, Fatmah Alshiajy, Fatima Abdelrahim, Hind Altag Alteraify Alsiddig, Lillian Mahfoud

{"title":"Immune thrombocytopenia as a rare initial manifestation and complication of Hodgkin lymphoma: a Pediatric case report.","authors":"Mohammad Obada Alsadi, Mohammed Swileh, Fatmah Alshiajy, Fatima Abdelrahim, Hind Altag Alteraify Alsiddig, Lillian Mahfoud","doi":"10.1093/omcr/omaf136","DOIUrl":"10.1093/omcr/omaf136","url":null,"abstract":"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 immune thrombocytopenia (ITP). Further evaluation revealed lymphadenopathy and splenomegaly. A biopsy of an axillary lymph node confirmed HL, with immunohistochemical analysis identifying Reed-Sternberg cells positive for CD30 and CD15. The patient began treatment with the ABVD chemotherapy regimen, resulting in significant clinical and hematological improvement. While ITP is commonly associated with autoimmune and lymphoproliferative disorders, its occurrence as a secondary complication of HL is rare, reported in less than 1% of cases. This case emphasizes the importance of considering HL as an underlying cause in patients presenting with unexplained ITP, particularly when lymphadenopathy or systemic symptoms are observed. Prompt diagnosis and initiation of therapy are crucial for achieving positive outcomes in such cases.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 8","pages":"omaf136"},"PeriodicalIF":0.4,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12365971/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Avascular necrosis as an uncommon manifestation in glycogen storage disease type III: diagnostic and therapeutic challenges. 缺血性坏死作为糖原储存病III型的不常见表现：诊断和治疗的挑战。

IF 0.4

Oxford Medical Case Reports Pub Date : 2025-08-20 eCollection Date: 2025-08-01 DOI: 10.1093/omcr/omaf145

Faiq I Gorial, Nabaa Ihsan Awadh, Sara S Khunda, Sajjad Ghanim Al-Badri, Ali Falah Alibrahimi

引用次数: 0