International Medical Case Reports Journal最新文献_第10页

Bilateral Chronic Herpetic Anterior Uveitis in an Immunocompetent Patient. 免疫功能正常患者的双侧慢性疱疹性前葡萄膜炎

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International Medical Case Reports Journal Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S490693

Jan Patrick Chu, Jagjit Singh Gilhotra

{"title":"Bilateral Chronic Herpetic Anterior Uveitis in an Immunocompetent Patient.","authors":"Jan Patrick Chu, Jagjit Singh Gilhotra","doi":"10.2147/IMCRJ.S490693","DOIUrl":"https://doi.org/10.2147/IMCRJ.S490693","url":null,"abstract":"Purpose: To present a case of bilateral herpes simplex anterior uveitis in an immunocompetent patient.Methods: Case Report.Results: A 42-year-old Kenyan female presented with a 2-year history of intermittent painful eye redness associated with blurring of vision of both eyes. Symptoms started after childbirth. There were no associated systemic symptoms. She presented with a best corrected visual acuity (BCVA) of 6/18 and 6/30 on the right and left eyes, respectively. On examination, conjunctival hyperaemia, large keratic precipitates (KPs), posterior synechiae, poorly dilating pupil, anterior subcapsular cataract and +2 anterior chamber (AC) cells and flare were noted on both eyes. Intraocular pressures (IOP) were within normal limits. Optical coherence tomography (OCT) showed bilateral cystoid macular oedema (CMO). Serum herpes simplex virus (HSV) IgM was detected, whereas autoimmune and other infectious aetiologies were excluded. Aqueous humour samples from both eyes tested negative for HSV. Bilateral 16 mg subtenon triamcinolone injection were done. Dexamethasone 0.1% eye drops and atropine 1.0% eye drops were started. Topical anti-glaucomatous medication was started due to IOP >30 mmHg on both eyes and Valacyclovir 1g three times a day was initiated. Final visit showed an improvement of BCVA to 6/9 on both eyes. There was complete resolution of AC cells and flare, and CMO on OCT.Conclusion: The diagnosis of bilateral herpetic anterior uveitis was based on the criteria set by The Herpetic Eye Disease Study (HEDS). Although the patient was immunocompetent, she was in a state of transient immunodeficiency that is pregnancy, which could have led to bilateral ocular involvement.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"913-918"},"PeriodicalIF":0.7,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11545606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142620462","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

Glucocorticoid-Induced Side Effects Cause Oral Lesions in Systemic Lupus Erythematosus: A Case Report. 糖皮质激素副作用导致系统性红斑狼疮口腔病变：病例报告

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International Medical Case Reports Journal Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S491296

Zulfa Fidi Pranadwista, Novia Tri Hasanah, Tenny Setiani Dewi, Wahyu Hidayat

{"title":"Glucocorticoid-Induced Side Effects Cause Oral Lesions in Systemic Lupus Erythematosus: A Case Report.","authors":"Zulfa Fidi Pranadwista, Novia Tri Hasanah, Tenny Setiani Dewi, Wahyu Hidayat","doi":"10.2147/IMCRJ.S491296","DOIUrl":"https://doi.org/10.2147/IMCRJ.S491296","url":null,"abstract":"Background: Systemic Lupus Erythematosus (SLE) is a complex autoimmune disease with various complications, making its management difficult. Glucocorticoid not only plays an essential role in the pathogenic therapy of SLE but also causes side effects such as oral lesions, especially when administered long-term or at high doses.Purpose: This case report aims to describe the management of glucocorticoid-induced side effects that cause oral lesions in SLE patient.Case presentation: A 30-year-old woman complained of a sore mouth and mouth-opening difficulty ten days prior. Previously, the patient complained of swelling in the legs and stomach, joint pain, hair loss, and skin redness on exposure to sunlight. Extra-oral examination revealed multiple red-black erosions and crusts on the zygoma region bilaterally over the nasal bridge, well-demarcated with an irregular shape, while the lips bled easily with hemorrhagic crusts that developed into serosanguineous crusts. Intra-oral examination showed scrapable white plaques on the palate, leaving erythematous areas, pain, and ulcers throughout the oral mucosa. The antinuclear antibody (ANA) examination revealed reactive results, positive anti-HSV-1 IgG, and positive hyphal on KOH examination. Based on the examination results, the diagnosis was SLE with herpes virus-associated oral involvement and acute pseudomembranous candidiasis.Case management: Comprehensive therapy, including non-pharmacological and pharmacological therapy, was involved. All oral lesions improved within one month.Conclusion: Various oral lesions may appear as manifestations of the disease and side effects of glucocorticoid therapy in SLE patients, thus requiring multidisciplinary monitoring and therapy from various fields.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"919-926"},"PeriodicalIF":0.7,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11545605/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142620464","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

Paralytic Ileus as the Initial Presentation of Guillain-Barre Syndrome: A Rare Case Report. 以麻痹性回肠炎为首发症状的格林-巴利综合征：罕见病例报告

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International Medical Case Reports Journal Pub Date : 2024-11-03 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S483673

Mohamed Farah Osman Hidig, Mohamed Sheikh Hassan, Abdiwahid Ahmed Ibrahim, Bakar Ali Adam, Nor Osman Sidow, Said Abdi Mohamed

{"title":"Paralytic Ileus as the Initial Presentation of Guillain-Barre Syndrome: A Rare Case Report.","authors":"Mohamed Farah Osman Hidig, Mohamed Sheikh Hassan, Abdiwahid Ahmed Ibrahim, Bakar Ali Adam, Nor Osman Sidow, Said Abdi Mohamed","doi":"10.2147/IMCRJ.S483673","DOIUrl":"https://doi.org/10.2147/IMCRJ.S483673","url":null,"abstract":"Emerging symmetrical limb weakness, altered sensory perception, and absent or reduced deep tendon reflexes are the hallmarks of Guillain-Barre syndrome (GBS). There are numerous studies that indicate up to two-thirds of patients with GBS may also have autonomic dysfunction. One uncommon presenting characteristic of GBS before motor weakness is evident is paralytic ileus, a sign of gastrointestinal dysautonomia. Here we describe the case of a 55-year-old man who was brought to the emergency room of our hospital with paralytic ileus, a less common symptom of early-stage GBS. The patient was initially treated with prokinetic drugs and total parenteral nutrition with no clinical improvement. The patient quickly developed ascending lower limb weakness that progressed to quadriplegia, which ultimately affected respiratory muscles, leading to respiratory failure requiring mechanical ventilation and intensive care unit hospitalization. A nerve conduction study showed demyelinating sensorimotor polyneuropathy. Analysis of cerebrospinal fluid revealed albumin-cytological dissociation. The patient was treated with intravenous immunoglobulin (IVIG) and other supportive treatments. Even though the patient's enteral feeding support was uncomfortable due to a profound infection complicating lack of stomach emptying during the hospital stay, the patient passed away two months after being admitted. Lack of awareness about GBS gastrointestinal dysautonomia may cause delays in treatment initiation, and as a result, GBS may lead to life-threatening events. Reducing mortality and morbidity from GBS requires prompt diagnosis and treatment. This case reminds us that GBS may present as gastrointestinal dysautonomia.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"909-912"},"PeriodicalIF":0.7,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11542473/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142604084","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

Pelvic Congestion Syndrome Related Vaginal Bleeding and the Efficacy of Transcatheter Foam Sclerotherapy in Managing This Condition: Two Case Reports. 盆腔充血综合征相关阴道出血及经导管泡沫硬化剂治疗的疗效：两个病例报告。

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International Medical Case Reports Journal Pub Date : 2024-11-02 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S490865

Haikun Yang, Yan Zhang, Wen He

{"title":"Pelvic Congestion Syndrome Related Vaginal Bleeding and the Efficacy of Transcatheter Foam Sclerotherapy in Managing This Condition: Two Case Reports.","authors":"Haikun Yang, Yan Zhang, Wen He","doi":"10.2147/IMCRJ.S490865","DOIUrl":"10.2147/IMCRJ.S490865","url":null,"abstract":"Pelvic congestion syndrome (PCS) is a chronic condition primarily characterized by pelvic pain and heaviness, with vaginal bleeding being a rare but significant symptom. We present two cases of PCS-related vaginal bleeding, emphasizing the necessity of considering PCS in differential diagnoses for abnormal vaginal bleeding. A 28-year-old Chinese woman presented with abnormal vaginal bleeding exacerbated by abdominal pressure during activities like squatting or defecation. Imaging revealed a dilated right ovarian vein, and transcatheter venography confirmed Nutcracker syndrome. After undergoing transcatheter foam sclerotherapy, her symptoms resolved. The second case involves a 29-year-old Chinese woman with similar symptoms; imaging and venography identified a dilated left ovarian vein. Following sclerotherapy, her symptoms also alleviated. These cases underscore the importance of recognizing PCS as a potential cause of abnormal vaginal bleeding and demonstrate the efficacy of transcatheter foam sclerotherapy in managing this condition. Integrating clinical presentation with imaging findings is crucial for timely diagnosis and effective treatment, ultimately improving patient outcomes.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"903-907"},"PeriodicalIF":0.7,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11539816/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142590984","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

Atypical Presentation of Choroidal Osteoma: Two Case Reports. 脉络膜骨瘤的非典型表现：两例报告

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International Medical Case Reports Journal Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S495500

Dafne Fernandes Machado, Stela Souza Peña, Mariana Carneiro Alves, Giovana Capecci Siqueira, Leonardo Amarante Pereira, Samantha Sanches de Carvalho, Thais Moura Gascon, Beatriz da Costa Aguiar Alves, Glaucia Luciano da Veiga, Fernando Luiz Affonso Fonseca, Vagner Loduca Lima, Priscilla Ballalai

{"title":"Atypical Presentation of Choroidal Osteoma: Two Case Reports.","authors":"Dafne Fernandes Machado, Stela Souza Peña, Mariana Carneiro Alves, Giovana Capecci Siqueira, Leonardo Amarante Pereira, Samantha Sanches de Carvalho, Thais Moura Gascon, Beatriz da Costa Aguiar Alves, Glaucia Luciano da Veiga, Fernando Luiz Affonso Fonseca, Vagner Loduca Lima, Priscilla Ballalai","doi":"10.2147/IMCRJ.S495500","DOIUrl":"10.2147/IMCRJ.S495500","url":null,"abstract":"Choroidal osteoma is a rare, benign, osseous choristoma presenting as an orange-yellow, well-defined fundus mass. It presents unilaterally in most cases, has a predilection for the female sex, and favor a juxtapapillary location, becoming clinically manifest when it involves the macula. Almost 60% of eyes with osteoma may suffer significant visual loss. Choroidal osteomas can easily be mistaken for other conditions with similar presentations. We herein report two rare cases presentation of choroidal osteoma: a 74-year-old male with 2-year blurred vision in the right eye (RE) initially misdiagnosed with age-related macular degeneration received intravitreal injections and after a multimodal evaluation, following cataract surgery in RE, confirmed to be choroidal osteoma and a 19-year-old female with a history of choroidal hemangioma presented with blurred vision in her left eye (LE), with examination revealed an irregular orange-yellow lesion along the superotemporal arcade with serous macular detachment, later diagnosed as choroidal osteoma.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"891-894"},"PeriodicalIF":0.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537187/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142583086","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

Community-Acquired Pneumonia with Acute Kidney Injury Complicated by Rhabdomyolysis- A Challenging Case Report in Resource Limit Setting. 社区获得性肺炎伴急性肾损伤并发横纹肌溶解症--资源有限环境下的挑战性病例报告。

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International Medical Case Reports Journal Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S492874

Ibrahim Abdullahi Mohamed, Abdullahi Abdirahman Omar, Mohamed Abdulahi Hassan, Omar Hassan Badawi

{"title":"Community-Acquired Pneumonia with Acute Kidney Injury Complicated by Rhabdomyolysis- A Challenging Case Report in Resource Limit Setting.","authors":"Ibrahim Abdullahi Mohamed, Abdullahi Abdirahman Omar, Mohamed Abdulahi Hassan, Omar Hassan Badawi","doi":"10.2147/IMCRJ.S492874","DOIUrl":"10.2147/IMCRJ.S492874","url":null,"abstract":"Background: Community-acquired pneumonia (CAP) is a common infectious disease that can lead to complications such as rhabdomyolysis (RM), a rare but potentially life-threatening condition involving muscle breakdown. RM can further complicate the clinical course by causing acute kidney injury (AKI). We present a case of Community-acquired pneumonia with AKI complicated by rhabdomyolysis in a resource-limited setting.Case presentation: A 67-year-old male presented with high fever, cough, and shortness of breath. He had no significant medical history. On examination, he was febrile, tachypneic, and tachycardic, with right-sided lung crackles. Lab tests showed elevated inflammatory markers and impaired kidney function. Chest radiography revealed right upper lobe consolidation, confirming pneumonia and AKI. He was treated with fluids, antibiotics, and supportive care, but his condition worsened, requiring intensive care unit (ICU). In the ICU, dark urine and elevated creatine kinase confirmed rhabdomyolysis. After aggressive fluid therapy and antibiotics the patient improved over six days and was transferred to the ward. By day 10, he fully recovered and was discharged with follow-up.Conclusion: This case underscores the importance of early recognition and prompt management of CAP complicated by AKI and rhabdomyolysis, even in resource-limited settings. Timely intervention can lead to favorable outcomes despite challenges.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"895-901"},"PeriodicalIF":0.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537182/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142583098","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

Influence of Placenta Extract Intake on Periodontal Diseases and Oral Environment: A Case Series. 摄入胎盘提取物对牙周病和口腔环境的影响：病例系列。

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International Medical Case Reports Journal Pub Date : 2024-10-26 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S487611

Hizuru Miyamoto, Kentarou Tahara, Eiichi Hirano

引用次数: 0

Vitamin a Deficiency in an Elderly Patient: A Diagnostic Challenge in the Age of AMD. 老年患者缺乏维生素 a：老年痴呆症时代的诊断挑战。

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International Medical Case Reports Journal Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S472944

Jakob M Pericak, Eric K Chin, David R P Almeida

引用次数: 0

The Improvement of Xerostomia and Reduction of Anxiety Score in a Patient with Generalized Anxiety Disorder and Recalcitrant Geographic Tongue: A Case Report and Literature Review. 改善广泛性焦虑症患者的口腔溃疡并降低其焦虑评分：病例报告与文献综述

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International Medical Case Reports Journal Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S480332

Nadia Tiara Putri, Faiznur Ridho, Indah Suasani Wahyuni

{"title":"The Improvement of Xerostomia and Reduction of Anxiety Score in a Patient with Generalized Anxiety Disorder and Recalcitrant Geographic Tongue: A Case Report and Literature Review.","authors":"Nadia Tiara Putri, Faiznur Ridho, Indah Suasani Wahyuni","doi":"10.2147/IMCRJ.S480332","DOIUrl":"10.2147/IMCRJ.S480332","url":null,"abstract":"Introduction: The incidence of post-pandemic psychiatric disorders has increased globally in recent decades. Generalized anxiety disorder (GAD) is one of the psychiatric disorders that are partially associated with emotional factors. It can affect the quantity and quality of saliva, present as xerostomia, and trigger the emergence of the geographic tongue (GT).Purpose: This case report aims to discuss the management of xerostomia and geographic tongue in a patient with GAD.Case: A 26-year-old male patient complained of dry and sore mouth for one month after taking medication from the psychiatry department, was diagnosed with GAD, and had already consumed the antidepressant sertraline. Extraoral examination showed dry and exfoliative lips. Intraoral examination showed white plaque with depapilation on the dorsal tongue, frothy saliva, buccal mucosa and dorsal tongue sticking to the dental mirror. The unstimulated salivary flow rate was <0.2 mL/min (sialometry method). The Depression, Anxiety, and Stress Scale-21 (DASS-21) questionnaire was used to estimate the psychological condition and showed an extremely severe level of anxiety (score = 13). The established oral diagnoses were GT with mild xerostomia and exfoliative cheilitis.Case management: For two months, patients received hyaluronic acid gel and mouthwash, as well as a non-pharmacological approach to healthy lifestyle counseling. There was an improvement in xerostomia, and the GT became asymptomatic, with a reduction of DASS score in this patient.Conclusion: Improved psychological conditions will improve xerostomia, but the clinical appearance of the geographic tongue is more difficult to eliminate.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"869-877"},"PeriodicalIF":0.7,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512784/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142500534","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

A Rare Case of Life-Threatening Jaundice Caused by Epstein-Barr Virus Infection and Secondary Cold Agglutinin Syndrome Successfully Treated with Rituximab. 用利妥昔单抗成功治疗由 Epstein-Barr 病毒感染引起的危及生命的黄疸和继发性冷凝集素综合征的罕见病例

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International Medical Case Reports Journal Pub Date : 2024-10-22 eCollection Date: 2024-01-01 DOI: 10.2147/IMCRJ.S477296

Matteo Bellia, Mariangela Greco, Monia Lunghi, Riccardo Moia, Gianluca Gaidano, Andrea Patriarca

{"title":"A Rare Case of Life-Threatening Jaundice Caused by Epstein-Barr Virus Infection and Secondary Cold Agglutinin Syndrome Successfully Treated with Rituximab.","authors":"Matteo Bellia, Mariangela Greco, Monia Lunghi, Riccardo Moia, Gianluca Gaidano, Andrea Patriarca","doi":"10.2147/IMCRJ.S477296","DOIUrl":"10.2147/IMCRJ.S477296","url":null,"abstract":"Background: Jaundice and hyperbilirubinemia are common clinical problems characterized by the presence of bile pigments in the blood and their deposition in body tissues. This clinical condition can be associated with a broad spectrum of potential benign and malignant causes, including hepatic inflammation, biliary obstruction, impaired bilirubin conjugation and bilirubin overproduction Therefore, the hyperbilirubinemia diagnostic work-up sometimes can be highly challenging and its therapeutic management can require a multidisciplinary approach.Case report: We report on a unique case of life-threatening jaundice and hepatic failure in a 20-year-old female who presented to the emergency room with complaints of fever, constant left abdominal pain and generalized profuse fatigue. A complete and detailed medical history, multiple tests for various infection, radiologic investigations and histological tests were performed in order to clarify the etiology of that rapidly progressive clinical condition. Based on the results, the patient jaundice was caused by an Epstein-Barr virus (EBV) infection and secondary cold agglutinin syndrome. Given the rare and complex diagnosis, multiple clinical specialists were asked to carry out the best patient management.Conclusion: This rare case highlights how challenging the differential diagnosis and treatment of hyperbilirubinemia can be, presenting a unique case of life-threatening multifactorial hepatic failure treated successfully with rituximab.","PeriodicalId":14337,"journal":{"name":"International Medical Case Reports Journal","volume":"17 ","pages":"861-867"},"PeriodicalIF":0.7,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512535/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142500532","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