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Post-Cardiac Injury Syndrome (Dressler Syndrome) Following Atrial Septal Defect (ASD) Repair: a Case Report 房间隔缺损(ASD)修复后心脏损伤综合征(Dressler综合征)一例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13090
A. Mirabi, Reihane Tabaraii, M. Sedaqat, Saba Gaeini, M. Masoumi
{"title":"Post-Cardiac Injury Syndrome (Dressler Syndrome) Following Atrial Septal Defect (ASD) Repair: a Case Report","authors":"A. Mirabi, Reihane Tabaraii, M. Sedaqat, Saba Gaeini, M. Masoumi","doi":"10.18502/crcp.v8i1.13090","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13090","url":null,"abstract":"Dressler syndrome is a type of secondary pericarditis that can be accompanied by pleural effusion or pericardial effusion resulting from injury of the pericardium or heart tissue. A 33-year-old male was admitted to the emergency department with pleuritic chest pain radiating to both shoulders and fever. Two months before the admission, the patient underwent traditional open-heart surgery with median sternotomy and pericardiectomy for atrial septal defect (ASD) closure. Blood tests showed elevated acute phase reactants (leukocytosis, high erythrocyte sedimentation rate, and C-reactive protein). Left-sided pleural effusion was revealed on chest CT scan. Diagnosis of Dressler syndrome was established. The patient’s pleuritic chest pain and shoulder pain improved clinically with a short course of colchicine. Although Dressler syndrome is rarely seen, it should be considered in the differential diagnosis of pleuritic chest pain. Special attention should be paid to Dressler’s syndrome because pericarditis can develop following cardiac surgery.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68126371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Severe diabetic ketoacidosis and coronavirus 2019 (COVID19) infection led to diagnosis of Autoimmune Polyglandular Syndrome 严重的糖尿病酮症酸中毒和冠状病毒2019 (covid - 19)感染导致诊断为自身免疫性多腺综合征
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13092
Meraj Tavakoli, S. Rabizadeh, Sara Seifouri, A. Esteghamati, M. Nakhjavani
{"title":"Severe diabetic ketoacidosis and coronavirus 2019 (COVID19) infection led to diagnosis of Autoimmune Polyglandular Syndrome","authors":"Meraj Tavakoli, S. Rabizadeh, Sara Seifouri, A. Esteghamati, M. Nakhjavani","doi":"10.18502/crcp.v8i1.13092","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13092","url":null,"abstract":"To this day, millions of people in the world have been diagnosed with corona virus 2019 (COVID-19). This disease cannot only lead to higher mortality rates among those with underlying Diabetes Mellitus (DM), but also may trigger DM in susceptible patients. Therefore, incidence of new-onset DM increased during the pandemic as a result; treatment of patients with diabetes and COVID-19 is important and needs further investigations. Here, we report a 27-year- old woman with past medical history of premature ovarian failure (POF) since14 years ago, who initially presented with severe diabetic ketoacidosis (DKA) which was triggered by COVID-19 and later through her lab results hypoparathyroidism was also detected. She was treated for DKA and COVID-19 Infection concomitantly, and she was also diagnosed with autoimmune polyglandular syndrome due to her multiple autoimmune endocrine organ involvements.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48766372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biliary Ascariasis with Gallbladder Invasion: A Unique Entity 胆道蛔虫病伴胆囊侵袭:一种独特的疾病
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13091
Manzoor Hussain, Nargis Banoo
{"title":"Biliary Ascariasis with Gallbladder Invasion: A Unique Entity","authors":"Manzoor Hussain, Nargis Banoo","doi":"10.18502/crcp.v8i1.13091","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13091","url":null,"abstract":"ntestinal Ascariasis is a common helminthic infection in developing countries and in some rare cases, worms migrate to the biliary tract and gall bladder. Extraintestinal biliary ascariasis presents with jaundice, right upper quadrant abdominal pain, and vomiting. Ultrasonography is a useful diagnostic modality. Albendazole and Mebendazole are commonly used anti-helmintic agents for conservative management, whereas endoscopic removal is needed in rare cases.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46488839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rhino-orbital Mucormycosis in an Immunocompetent Pediatric Patient, Resembling an Orbital Mass- a Case Report 一例具有免疫功能的儿童患者的鼻腔眼眶毛霉菌病，类似眼眶肿块-病例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13101
S. M. Rafizadeh, M. Aminizade, F. A. Amoli, M. Anari, M. Khodabandeh, Abbas Mohammadi
{"title":"Rhino-orbital Mucormycosis in an Immunocompetent Pediatric Patient, Resembling an Orbital Mass- a Case Report","authors":"S. M. Rafizadeh, M. Aminizade, F. A. Amoli, M. Anari, M. Khodabandeh, Abbas Mohammadi","doi":"10.18502/crcp.v8i1.13101","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13101","url":null,"abstract":"Rhino-orbital mucormycosis in an immunocompetent pediatric patient can present as an orbital mass. We report a 9-year-old male that presented with periorbital swelling and limitation of left eye movement from one month ago. The patient was treated at another center with a diagnosis of mucormycosis but was referred due to worsening symptoms. Orbital and paranasal sinus CT scan revealed opacities in the left paranasal sinus and soft tissue density in the medial and inferior orbital wall. The patient underwent orbitotomy and mass debulking surgery on suspicion of a possible neoplastic mass. Pathologic evaluations revealed mucormycosis. After receiving intravenous liposomal amphotericin-B that was followed by oral posaconazole syrup for two months and sinus debridement, the symptoms regressed. In immunocompromised pediatric patients, mucormycosis should be considered in the differential diagnosis of an orbital mass.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45056878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
a Case of COVID-19 with No Pulmonary Involvement; but with Mediastinal and Subcutaneous Emphysema 一例无肺部受累的新冠肺炎病例；但伴有纵隔和皮下肺气肿
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12272
Hamid Talebzadeh, Sadegh Mazaheri-Tehrani, Mohammad Fakhrolmobasheri
{"title":"a Case of COVID-19 with No Pulmonary Involvement; but with Mediastinal and Subcutaneous Emphysema","authors":"Hamid Talebzadeh, Sadegh Mazaheri-Tehrani, Mohammad Fakhrolmobasheri","doi":"10.18502/crcp.v7i6.12272","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12272","url":null,"abstract":"Spontaneous pneumomediastinum (SPM) is a rare clinical entity. In the normal population, it is more likely to occur in people with conditions including chronic obstructive pulmonary diseases and asthma. In the context of COVID-19 few cases of SPM have been reported which most of them were patients with severe lung parenchymal inflammation or patients under mechanical ventilation. In this case, we report a young male with a history of minor childhood asthma who presented with acute dyspnea, forceful coughs, and subcutaneous emphysema. Chest computed tomography had no clues for COVID-19, however, pneumomediastinum and subcutaneous emphysema were obvious. He was primarily diagnosed with acute asthma exacerbation causing SPM but eventually, he tested positive for SARS-COV-2, therefore, he underwent the standard treatment for COVID-19 and the SPM was managed conservatively. Finally, after 12 days of hospitalization, he was discharged in favorable clinical condition.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48120577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tuberculous Arthritis: A Forgotten Diagnosis During Pandemic Covid-19 结核性关节炎：新冠肺炎大流行期间被遗忘的诊断
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12268
T. Huwae, A. Pribadi
{"title":"Tuberculous Arthritis: A Forgotten Diagnosis During Pandemic Covid-19","authors":"T. Huwae, A. Pribadi","doi":"10.18502/crcp.v7i6.12268","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12268","url":null,"abstract":"Tuberculosis (TB) is a respiratory disease that primarily affects the lungs. The challenge is to recognize the characteristic of TB disease, including extrapulmonary presentation. TB arthritis is an extrapulmonary TB presentation in the joint, which is frequently neglected and misdiagnosed. A 41-year-old female patient was presented with a major complaint of chronic pain in her left wrist for three months. The patient had a low-grade fever without respiratory symptoms. Local examination revealed swelling, warmth and tenderness. Erythrocyte sedimentation rate (ESR) was increased and chest radiograph demonstrated pulmonary TB. She underwent arthrotomy debridement and culture examination. We initiated adjuvant anti-tuberculous treatment. On the evaluation, she reported relief from pain and showed improvement in general condition. TB arthritis is unique due to its rare incidence and unspecific clinical manifestations. A better understanding of these issues will prevent possible diagnostic errors. Prompt treatment was crucial to maintain joint function and prevent permanent destruction.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41554436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Misoprostol is Useful for Post Cesarean Section Management of Redo Syndrome 米索前列醇可用于剖宫产后再造综合征的治疗
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12275
A. D. Shahraki, Azam Zafarbakhs, Amirreza Farhadian Dehkordi, Taherh Khalili Brojeni, F. Haghollahi
{"title":"Misoprostol is Useful for Post Cesarean Section Management of Redo Syndrome","authors":"A. D. Shahraki, Azam Zafarbakhs, Amirreza Farhadian Dehkordi, Taherh Khalili Brojeni, F. Haghollahi","doi":"10.18502/crcp.v7i6.12275","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12275","url":null,"abstract":"Redo syndrome or acute hematometra is a rare complication after abortion or cesarean section.A-32- year-old woman with previous cesarean section, term pregnancy, and labor pain referred to hospital.She delivered a healthy baby with a good Apgar score and discharge 2 days later without complications after a cesarean section. She came back to the hospital with the severe abdominal pain, weakness, without abnormal bleeding, at 6 days postpartum. Abdominopelvic sonography showed a large hematometra in the uterus. She took misoprostol 200 μg intra vaginal and 200μg sublingual, plus serum oxytocin and cefazolin. After about 1.5 hours, she passed a large hematoma, her pain gradually relieved, and she was discharged three days later. This report show that misoprostol is useful in the management of acute hematometra.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42919796","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Familial Neuromyelitis Optica: A Case Report and Literature Review 家族性视神经脊髓炎1例报告及文献复习
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12276
Z. Ebadi, F. Ghadiri, E. Asadollahzade, A. Moghadasi
{"title":"Familial Neuromyelitis Optica: A Case Report and Literature Review","authors":"Z. Ebadi, F. Ghadiri, E. Asadollahzade, A. Moghadasi","doi":"10.18502/crcp.v7i6.12276","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12276","url":null,"abstract":"Neuromyelitis Optica Spectrum Disorder (NMOSD) is an autoimmune rare disorder that involves the endfeet of astrocytes. The role of genetics in the disease is not well known. Rare cases of familial NMOSD were reported worldwide. In this report, first, we presented a young man with myelitis and his cousin who suffered from this disease. Then we reviewed some reports around the world about familial NMO. The prevalence of familial NMO is nearly 3%. First cases are reported from East Asia. Its characteristics are similar to the sporadic type. Recent data suggest genetics play role in NMO.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46237543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
a Case of COVID-19 and Tuberculous Meningitis Coinfection 新冠肺炎并发结核性脑膜炎1例
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12269
Shaghayegh Ashraf Talesh, Sara Zare, A. Hadadi
{"title":"a Case of COVID-19 and Tuberculous Meningitis Coinfection","authors":"Shaghayegh Ashraf Talesh, Sara Zare, A. Hadadi","doi":"10.18502/crcp.v7i6.12269","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12269","url":null,"abstract":"Neurological symptoms like headache have been reported in patients infected with tuberculosis (TB) and COVID-19 infection [1]. A high index of suspicions is necessary for diagnosing of COVID-19 and neurologic tuberculous coinfection, particularly in the communities at high risk for TB or in an endemic region. Herein, we report a case of a 60-year-old man diagnosed with acute COVID-19 and tuberculous meningitis coinfection, to emphasize challenges about this coinfection, because underlying lung diseases like latent TB will affect the clinical categorization (for severity) of COVID-19, and then active TB disease may severe illness.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43349711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rhino-Sino-Cerebral Mucormycosis Associated with Long-Term Rituximab Therapy in Multiple Sclerosis: A Case Report and Review of the Literature 多发性硬化症长期利妥昔单抗治疗相关的鼻-脑毛霉菌病:1例报告和文献回顾
Case Reports in Clinical Practice Pub Date : 2023-03-15 DOI: 10.18502/crcp.v7i6.12278
Mohsen Koosha, Golfam Mehrparvar, Sepideh Paybast
{"title":"Rhino-Sino-Cerebral Mucormycosis Associated with Long-Term Rituximab Therapy in Multiple Sclerosis: A Case Report and Review of the Literature","authors":"Mohsen Koosha, Golfam Mehrparvar, Sepideh Paybast","doi":"10.18502/crcp.v7i6.12278","DOIUrl":"https://doi.org/10.18502/crcp.v7i6.12278","url":null,"abstract":"Introduction: Rituximab is a CD20 depleting agent, widely used as an off-label diseasemodifying treatment (DMT) in treating multiple sclerosis (MS). The present study aimed to report the first case of rhino-sino-cerebral mucormycosis in a patient with secondary progressive MS (SPMS), treated with rituximab. \u0000Case Report: The patient was a 38-year-old man with a history of SPMS treated with rituximab, who developed subacute left vision loss and impaired ocular movement. He also mentioned a concomitant severe headache and cheek swelling. Based on the brain and orbital magnetic resonance imaging (MRI) findings, rhino-sino-cerebral mucormycosis was suspected. Subsequent endoscopic examination confirmed the diagnosis. He underwent medical treatment with amphotericin B liposomal and surgical debridement leading to a significant clinical recovery. He was eventually discharged home with a solid recommendation to discontinue rituximab. \u0000Conclusion: The present report indicates a case of SPMS treated with rituximab, who developed rhino-sino-cerebral mucormycosis.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42327046","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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