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Unilateral Periorbital Swelling in a Pediatric Patient. 一名儿科患者的单侧眶周肿胀
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-31 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241255563
Ana Rosas Herrera, Ashley B Parker, Mark Chaskes, Frederic Askin, Aurelia S Monk, John R Stephens, Brian D Thorp, Charles S Ebert, Brent A Senior, Adam J Kimple, Keonho A Kong
{"title":"Unilateral Periorbital Swelling in a Pediatric Patient.","authors":"Ana Rosas Herrera, Ashley B Parker, Mark Chaskes, Frederic Askin, Aurelia S Monk, John R Stephens, Brian D Thorp, Charles S Ebert, Brent A Senior, Adam J Kimple, Keonho A Kong","doi":"10.1177/11795476241255563","DOIUrl":"10.1177/11795476241255563","url":null,"abstract":"<p><p>Infratemporal fossa (ITF) tumors are rare in children and may present with a variety of symptoms. Teratomas are neoplasms derived from the 3 germ layers and approximately 6% to 10% are within the head and neck. Our study discusses one of the first reported cases of teratoma in the ITF in a pediatric patient. A 3-year-old girl presents with 2 years of recurrent monthly left periorbital swelling accompanied by fevers, skin discoloration, and pain. Prior episodes were treated with antibiotics with incomplete resolution. Imaging revealed a cystic lesion centered in the ITF. She was taken for endoscopic endonasal biopsy of the lesion and had no complications. Pathology revealed a mature teratoma composed primarily of pancreatic tissue. Providers should consider masses such as teratoma in the differential for ITF tumors and periorbital edema unresponsive to typical treatment.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241255563"},"PeriodicalIF":1.0,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11143867/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141199560","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
Corrigendum to "Blue Rubber Bleb Nevus Syndrome Presenting as Anemia, Hemorrhage, and Hemangiomas: A Rare Case Report". 以贫血、出血和血管瘤为表现的蓝色橡胶痣综合征：罕见病例报告 "的更正。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-24 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241256213
{"title":"Corrigendum to \"Blue Rubber Bleb Nevus Syndrome Presenting as Anemia, Hemorrhage, and Hemangiomas: A Rare Case Report\".","authors":"","doi":"10.1177/11795476241256213","DOIUrl":"https://doi.org/10.1177/11795476241256213","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1177/11795476231173503.].</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241256213"},"PeriodicalIF":1.0,"publicationDate":"2024-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11127569/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141154455","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
Superior Mesenteric Artery Syndrome in an 11-Year-Old Boy: A Case Report. 一名 11 岁男孩的肠系膜上动脉综合征：病例报告。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-23 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241257036
Sakar Babu Gharti, Nischal Shrestha, Kaushal Samsher Thapa, Rajat Shah, Priti Khanal, Rajnish Kumar Shah, Sanjeeb Babu Gharti, Umesh Tiwari
{"title":"Superior Mesenteric Artery Syndrome in an 11-Year-Old Boy: A Case Report.","authors":"Sakar Babu Gharti, Nischal Shrestha, Kaushal Samsher Thapa, Rajat Shah, Priti Khanal, Rajnish Kumar Shah, Sanjeeb Babu Gharti, Umesh Tiwari","doi":"10.1177/11795476241257036","DOIUrl":"10.1177/11795476241257036","url":null,"abstract":"<p><p>Superior Mesenteric Artery Syndrome (SMAS) is a rare but potentially life-threatening condition caused by the compression of the duodenum by the superior mesenteric artery. We report a case of an 11-year-old male who complaint of abdominal pain and intermittent vomiting for last 3 weeks. Diagnosis of SMAS was made with the help of radiological findings. The patient was managed conservatively with nutritional support, prokinetic agents, and stomach decompression. After 2 weeks of treatment, the patient's symptoms improved, and he was discharged from the hospital.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241257036"},"PeriodicalIF":1.0,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11119349/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141154490","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
Polyneuropathy as an initial manifestation of Hereditary Transtyretin Amyloidosis (ATTRV) in a young patient: Case report of a diagnostic challenge. 一名年轻患者的多发性神经病是遗传性经丝体淀粉样变性（ATTRV）的最初表现：诊断难题的病例报告。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-15 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241253106
Julieth Vivian Sarmiento Palma, Santiago Sambracos Parrado, Maria Camila Echeverria, Paula Ruiz Talero
{"title":"Polyneuropathy as an initial manifestation of Hereditary Transtyretin Amyloidosis (ATTRV) in a young patient: Case report of a diagnostic challenge.","authors":"Julieth Vivian Sarmiento Palma, Santiago Sambracos Parrado, Maria Camila Echeverria, Paula Ruiz Talero","doi":"10.1177/11795476241253106","DOIUrl":"https://doi.org/10.1177/11795476241253106","url":null,"abstract":"<p><p>We report the case of a 27-year-old man with transthyretin amyloidosis secondary to the p.Val142Ile mutation with an atypical clinical presentation of predominantly lower limb polyneuropathy without cardiac involvement. p.Val142Ile is mainly associated with cardiopathy, whereas the neuropathic phenotype is mainly associated with p.Val50Met. Our patient belongs to a non-endemic region and due to his lack of support network a possible familial component is unknown. His case represents a diagnostic challenge given the wide heterogeneity of clinical manifestations associated with the disease, with other possible diagnoses of polyneuropathy being reasonably excluded according to prevalence and frequency. The particularly unusual genotype-phenotype association distinguishes this case from the classic description of transthyretin amyloidosis secondary to p.Val142Ile.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241253106"},"PeriodicalIF":1.0,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11097722/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140956213","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
Surgical Myectomy and Myotomy for Refractory Blepharospasm in Meige Syndrome Patients: A Case Report. 梅杰综合征患者难治性眼睑痉挛的肌层切除术和肌切开术：病例报告。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-14 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241254266
Ming-Ming Li, Zhi-Min Cen, Huang Zhang, Zhong-Ling Luo
{"title":"Surgical Myectomy and Myotomy for Refractory Blepharospasm in Meige Syndrome Patients: A Case Report.","authors":"Ming-Ming Li, Zhi-Min Cen, Huang Zhang, Zhong-Ling Luo","doi":"10.1177/11795476241254266","DOIUrl":"10.1177/11795476241254266","url":null,"abstract":"<p><p>Meige syndrome is a rare neurological disease characterized by segmental dystonia, specifically blepharospasm and oromandibular dystonia. These symptoms are often accompanied by complex movements of the eyelids, lower facial muscles, mandible, and neck muscles. Bilateral blepharospasm is the most common feature of this disease. In this case report, we present the successful treatment of refractory blepharospasm in a 72-year-old woman with Meige syndrome via 2 incisions resulting from myectomy and in situ surgery.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241254266"},"PeriodicalIF":1.0,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11095178/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140943167","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 Case Report of Asthma Exacerbation Induced by Excessive Drinking Water. 过量饮水诱发哮喘加重的病例报告
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-12 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241253107
Shunxin Lv, Huachen Jiao, Ying Qu, Mengdi Zhang, Rui Wang, Yan Li, Feng Jiang, Laiyun Xin
{"title":"A Case Report of Asthma Exacerbation Induced by Excessive Drinking Water.","authors":"Shunxin Lv, Huachen Jiao, Ying Qu, Mengdi Zhang, Rui Wang, Yan Li, Feng Jiang, Laiyun Xin","doi":"10.1177/11795476241253107","DOIUrl":"10.1177/11795476241253107","url":null,"abstract":"<p><p>Excessive water consumption is an extremely rare and potential asthma risk factor with very few cases reported in the literature. Common triggers of asthma include genetic factors, smoking, allergens, and viral respiratory infections. The adult patient with asthma reportedly drank too much water and was unable to get relief from his asthma while hospitalized. The patient's asthma was better controlled with the use of diuretics and control of the patient's fluid intake and output. This case explores asthma induced by excessive drinking of water.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241253107"},"PeriodicalIF":1.0,"publicationDate":"2024-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11092540/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140921604","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
Idiopathic Granulomatous Vulvitis: A Case Report on a Rare Disease. 特发性肉芽肿性外阴炎：罕见疾病的病例报告
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-08 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241253109
Jihan M Muhaidat, Enas A Alhaje, Firas A Al-Qarqaz, Diala M Alshiyab, Almutazballlah Bassam Qablan
{"title":"Idiopathic Granulomatous Vulvitis: A Case Report on a Rare Disease.","authors":"Jihan M Muhaidat, Enas A Alhaje, Firas A Al-Qarqaz, Diala M Alshiyab, Almutazballlah Bassam Qablan","doi":"10.1177/11795476241253109","DOIUrl":"10.1177/11795476241253109","url":null,"abstract":"<p><p>Idiopathic granulomatous vulvitis is an uncommon anogenital area disease described in the last few decades. It causes an inflammatory reaction that culminates in swelling and possibly distortion of the female anogenital area. Many reported cases consider this non-infectious entity the genital counterpart to granulomatous cheilitis. We here present a 64 years old female patient with idiopathic granulomatous vulvitis co-existing with lipodermatosclerosis, with the excellent response of the former condition to hydroxychloroquine and potent topical steroids.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241253109"},"PeriodicalIF":1.0,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11080743/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140897447","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
Primary Tuberculosis of the Pharynx in an HIV Context: A Case Report. 艾滋病毒背景下的原发性咽部结核病：病例报告。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-05 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241251945
Cristian Morán-Mariños, Felix Llanos-Tejada, Renzo Villanueva-Villegas, Kanneth G Vargas-Ponce, Juan Salas-López
{"title":"Primary Tuberculosis of the Pharynx in an HIV Context: A Case Report.","authors":"Cristian Morán-Mariños, Felix Llanos-Tejada, Renzo Villanueva-Villegas, Kanneth G Vargas-Ponce, Juan Salas-López","doi":"10.1177/11795476241251945","DOIUrl":"10.1177/11795476241251945","url":null,"abstract":"<p><p>Pharyngeal tuberculosis without pulmonary involvement is very rare and may be confused with malignant lesions. We present a 45-year-old female patient with a history of HIV presenting with a history of cough, sore throat, and oral ulcers with chronic use of antibiotics. The evolution would indicate a probable malignant tumor, but the biopsy was consistent with Pharyngeal TB. The patient initiated anti-tuberculosis therapy and demonstrated improved conditions and remission of ulcers. In the context of HIV, this treatment could be a major contributor to the underdiagnosis of the disease and may lead to alternative diagnoses. Therefore, it is vital to consider this condition in patients who do not respond to antibiotics.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241251945"},"PeriodicalIF":1.0,"publicationDate":"2024-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11072070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140862291","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
Kartagener's Syndrome Complicated by Bronchiectasis with Tricuspid and Mitral Valve Regurgitation: A Case Report. 支气管扩张并发三尖瓣和二尖瓣反流的卡塔格纳综合征：病例报告
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-05-03 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241251940
Rayyan Vaid, Areeba Fareed, Maaz Ahmad Siddiqui
{"title":"Kartagener's Syndrome Complicated by Bronchiectasis with Tricuspid and Mitral Valve Regurgitation: A Case Report.","authors":"Rayyan Vaid, Areeba Fareed, Maaz Ahmad Siddiqui","doi":"10.1177/11795476241251940","DOIUrl":"https://doi.org/10.1177/11795476241251940","url":null,"abstract":"<p><strong>Background: </strong>Kartagener's syndrome, a rare autosomal recessive genetic disorder, is characterized by primary ciliary dyskinesia (PCD), resulting in defective cilia function in the respiratory tract and fallopian tubes.</p><p><strong>Case presentation: </strong>This case report discusses a 23-year-old female with Kartagener's syndrome, bronchiectasis, and cardiac involvement, who presented with shortness of breath, cough, and syncope. Notably, she received home oxygen therapy but became exhausted, leading to loss of consciousness. Clinical examination revealed prominent heart sounds and abnormal lung findings. Laboratory results indicated leukocytosis, and an ECG confirmed dextrocardia and cardiac abnormalities. Doppler studies identified mitral and tricuspid regurgitation along with severe pulmonary arterial hypertension. Antibiotics were administered for coagulase-negative Staphylococcus infection. The patient improved with a treatment regimen, including oxygenation and nebulization. Regular follow-up and patient education were emphasized.</p><p><strong>Conclusion: </strong>This case underscores the complexity of Kartagener's syndrome and the importance of a multidisciplinary approach in managing its respiratory and cardiac manifestations.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241251940"},"PeriodicalIF":1.0,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11069330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140850651","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
Treatment With a Patented 3.6:1 Myo-Inositol to D-chiro-Inositol Ratio, Antioxidants, Vitamins and Minerals Food Supplement in Women With a History of Assisted Reproductive Technique (ART) Failures: A Series of Case Reports. 在有辅助生殖技术（ART）失败史的妇女中使用 3.6:1 肌醇与 D-chiro-Inositol 比率的专利肌醇、抗氧化剂、维生素和矿物质食品补充剂进行治疗：系列病例报告。
IF 1
Clinical Medicine Insights. Case Reports Pub Date : 2024-03-29 eCollection Date: 2024-01-01 DOI: 10.1177/11795476241242265
A Armijo-Sánchez, N Benítez Castillo, E García-Vidal, M Luna Chadid, C Salvador Ballada, G Valls Ricart, V Torres Pellens
{"title":"Treatment With a Patented 3.6:1 Myo-Inositol to D-chiro-Inositol Ratio, Antioxidants, Vitamins and Minerals Food Supplement in Women With a History of Assisted Reproductive Technique (ART) Failures: A Series of Case Reports.","authors":"A Armijo-Sánchez, N Benítez Castillo, E García-Vidal, M Luna Chadid, C Salvador Ballada, G Valls Ricart, V Torres Pellens","doi":"10.1177/11795476241242265","DOIUrl":"10.1177/11795476241242265","url":null,"abstract":"<p><p>Infertility affects 15% of couples in reproductive age worldwide. In women in particular, infertility can be caused by various abnormalities, with polycystic ovary syndrome (PCOS) being the most common. Currently, there are many assisted reproductive techniques (ART) available to combat the burden of infertility. However, positive results are not guaranteed. The administration of inositol has been shown to increase positive reproductive outcomes in women undergoing ART. Here we present a series of clinical cases in which women with a history of infertility and previously failed ART, supplemented with a specific 3.6:1 MYO:DCI ratio, antioxidants, vitamins, and minerals for a period of 1 to 3 months before undergoing <i>in vitro</i> fertilization (IVF). In this series of case reports, we provide preliminary evidence that supplementation with a specific 3.6:1 MYO to DCI ratio, as well as antioxidants, vitamins, and minerals may contribute positively to female fertility in women undergoing IVF, with a history of primary or secondary infertility and previously failed ART.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. Case Reports","volume":"17 ","pages":"11795476241242265"},"PeriodicalIF":1.0,"publicationDate":"2024-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10981332/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140334933","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
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