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Non-Vital Decoronation of a Maxillary Central Incisor: A Case Report With 18 Months Follow-Up 上颌中切牙非生命性装饰1例，随访18个月
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.70913
Maryam Enteghad, Zahra Lotf Haghpanah
{"title":"Non-Vital Decoronation of a Maxillary Central Incisor: A Case Report With 18 Months Follow-Up","authors":"Maryam Enteghad,&nbsp;Zahra Lotf Haghpanah","doi":"10.1002/ccr3.70913","DOIUrl":"https://doi.org/10.1002/ccr3.70913","url":null,"abstract":"<p>In the present case, decoronation and root submergence of a necrotic maxillary central incisor were performed for a 13-year-old girl. The root canal was filled with mineral trioxide aggregate (MTA), which was covered with resin-modified glass ionomer. Apexification with MTA was performed for her other maxillary central incisor, and the edentulous region was restored using a fiber-reinforced composite bridge. Long-term follow-up indicated that decoronation might be a viable option to maintain the alveolar bone.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.70913","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145223999","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
Haloperidol Induced Orofacial Dyskinesia: Clinical Insights Into Buccolingual Masticatory Syndrome 氟哌啶醇诱导的口腔面部运动障碍：颊舌咀嚼综合征的临床观察
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71083
Gudisa Bereda
{"title":"Haloperidol Induced Orofacial Dyskinesia: Clinical Insights Into Buccolingual Masticatory Syndrome","authors":"Gudisa Bereda","doi":"10.1002/ccr3.71083","DOIUrl":"https://doi.org/10.1002/ccr3.71083","url":null,"abstract":"<p>Haloperidol and other antipsychotics can cause buccolingual masticatory syndrome (BLMS), a rare but serious extrapyramidal disorder characterized by involuntary movements of the cheeks, jaws, and tongue. The author describes a 40-year-old man presenting with retrograde lingual movements, chewing difficulties, and speech impairment after 2 years of haloperidol therapy for catatonic-type schizophreniform disorder. Magnetic resonance imaging showed abnormal activity in the basal ganglia without structural lesions. Treatment with oral trihexyphenidyl hydrochloride, 5 mg daily, resulted in symptom resolution within 24 h. Haloperidol induces motor dysfunction by blocking dopamine D2 receptors in the basal ganglia. Haloperidol was discontinued, and the patient was transitioned to clozapine, a second-generation antipsychotic with a lower risk of tardive dyskinesia. Clozapine was initiated at 12.5 mg daily and titrated to 50 mg daily over two weeks, following standard hematologic monitoring protocols. Early diagnosis and appropriate management, including medication adjustment and adjunctive therapy, are critical to optimizing outcomes.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71083","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145224036","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 on the Open Surgical Repair of Thoracoabdominal Aortic Aneurysm With Severe Thoracic Vertebral Body Erosion. Experience in LMIC 胸腹主动脉瘤开放性修复伴严重胸椎体糜烂1例报告。LMIC经验
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71115
Natnael G. Admassu, Chernet T. Mengistie, Biruk T. Mengistie, Solyana Bereded, Yonas Nibret, Henok Teklesilase, Abebe Bezabh, Azaryas K. Admassu
{"title":"A Case Report on the Open Surgical Repair of Thoracoabdominal Aortic Aneurysm With Severe Thoracic Vertebral Body Erosion. Experience in LMIC","authors":"Natnael G. Admassu,&nbsp;Chernet T. Mengistie,&nbsp;Biruk T. Mengistie,&nbsp;Solyana Bereded,&nbsp;Yonas Nibret,&nbsp;Henok Teklesilase,&nbsp;Abebe Bezabh,&nbsp;Azaryas K. Admassu","doi":"10.1002/ccr3.71115","DOIUrl":"https://doi.org/10.1002/ccr3.71115","url":null,"abstract":"<p>Open surgical repair of thoracoabdominal aortic aneurysm with vertebral erosion is rare and complex, especially in low-resource settings. This case shows that with multidisciplinary planning, staged aneurysm exclusion and spinal stabilization can yield excellent outcomes, even where endovascular tools are unavailable.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71115","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145224112","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
Omental Cystic Lymphangioma as a Rare Abdominal Tumor: A Case Report and Literature Review 网膜囊性淋巴管瘤是一种罕见的腹部肿瘤：1例报告及文献复习
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71107
Ali Mirsadeghi, Sina Esmailpour, Arefeh Moballegh, Farnood Forouhar, Narges Mesbah
{"title":"Omental Cystic Lymphangioma as a Rare Abdominal Tumor: A Case Report and Literature Review","authors":"Ali Mirsadeghi,&nbsp;Sina Esmailpour,&nbsp;Arefeh Moballegh,&nbsp;Farnood Forouhar,&nbsp;Narges Mesbah","doi":"10.1002/ccr3.71107","DOIUrl":"https://doi.org/10.1002/ccr3.71107","url":null,"abstract":"<p>We report the case of a 30-year-old man who experienced intermittent abdominal pain for 1.5 years. He presented with worsening pain during defecation and bladder filling. A CT scan revealed a large abdominal cystic lesion, along with smaller cysts in the pelvis. Surgical resection of the cystic lesions was performed via laparotomy, which also included an appendectomy and omentectomy. Histopathological analysis confirmed the diagnosis of cystic lymphangiomas.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71107","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145223927","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
Adult Case of Congenital Intratympanic Membrane Cholesteatoma 成人先天性鼓膜胆脂瘤1例
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71072
Jumpei Fukui, Ichiro Fukumoto, Keiichi Koshizuka, Tomohisa Iinuma, Kazuki Yamasaki, Shuji Yonekura, Toshimitsu Nemoto, Toyoyuki Hanazawa
{"title":"Adult Case of Congenital Intratympanic Membrane Cholesteatoma","authors":"Jumpei Fukui,&nbsp;Ichiro Fukumoto,&nbsp;Keiichi Koshizuka,&nbsp;Tomohisa Iinuma,&nbsp;Kazuki Yamasaki,&nbsp;Shuji Yonekura,&nbsp;Toshimitsu Nemoto,&nbsp;Toyoyuki Hanazawa","doi":"10.1002/ccr3.71072","DOIUrl":"https://doi.org/10.1002/ccr3.71072","url":null,"abstract":"<p>Intratympanic membrane cholesteatoma (ITMC) is a rare type of cholesteatoma located within the tympanic membrane. Surgery is a treatment option if the ITMCs do not spontaneously disappear. Transcanal endoscopic ear surgery is anticipated to become the standard approach in the future.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71072","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145223929","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
Life-Threatening Esophageal Injury From Sword Swallowing, Courage and Caution in Respecting Life: A Case Study of an 18-Year-Old Acrobat 吞剑致食道致命损伤，尊重生命的勇气与谨慎：一名18岁杂技演员的个案研究
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71090
Yun Cao, Jiaqi Zhang, Aixia Gong
{"title":"Life-Threatening Esophageal Injury From Sword Swallowing, Courage and Caution in Respecting Life: A Case Study of an 18-Year-Old Acrobat","authors":"Yun Cao,&nbsp;Jiaqi Zhang,&nbsp;Aixia Gong","doi":"10.1002/ccr3.71090","DOIUrl":"https://doi.org/10.1002/ccr3.71090","url":null,"abstract":"<p>An 18-year-old acrobat suffered esophageal perforation during sword swallowing. Preoperative CT showed pneumomediastinum and subcutaneous emphysema, but no perforation location. A novel endoscopic technique using a clear cap and air/water shutoff successfully localized a 1.0 cm posterior esophageal perforation without active bleeding, enabling successful surgery and patient survival.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71090","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145224000","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
Adult-Onset Partial Unilateral Lentiginosis: A Rare Pigmentary Mosaicism With Clinical Response to Tranexamic Acid 成人发病的部分单侧黄斑病：一种罕见的色素镶嵌病，对氨甲环酸有临床反应
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.71113
Niranjan Pudasaini, Sabin Poudel, Aashutosh Pokharel, Anup Mishra, Anil Kumar Singh Dangol, Manisha Chapagain
{"title":"Adult-Onset Partial Unilateral Lentiginosis: A Rare Pigmentary Mosaicism With Clinical Response to Tranexamic Acid","authors":"Niranjan Pudasaini,&nbsp;Sabin Poudel,&nbsp;Aashutosh Pokharel,&nbsp;Anup Mishra,&nbsp;Anil Kumar Singh Dangol,&nbsp;Manisha Chapagain","doi":"10.1002/ccr3.71113","DOIUrl":"https://doi.org/10.1002/ccr3.71113","url":null,"abstract":"<p>Partial unilateral lentiginosis (PUL) is a rare pigmentary disorder characterized by numerous lentigines grouped within normal skin in a segmental pattern with sharp demarcation at the midline. The authors hereby present a case of a 40-year-old female, who presented with multiple asymptomatic, gradually progressive, brownish flat skin lesions on her left breast, abdomen, and left half of the trunk for 16 years. Diagnosis was made clinically via properly documented history, physical examination, and histopathological evaluation. Although treatment is unnecessary, many patients seek consultations for cosmetic reasons. Our patient is showing a good response to the prescribed tablet tranexamic acid and topical kojic acid cream, along with regular application of sun protection cream SPF 50+. This is a rare case of adult-onset PUL showing good clinical improvement with oral tranexamic acid combined with kojic acid cream.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.71113","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145224109","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
Osteomyelitis as a Rare Complication in an 8-Year-Old Boy With Beta Thalassemia: A Case Report 骨髓炎是一种罕见的并发症在8岁男孩β地中海贫血：1例报告
IF 0.6
Clinical Case Reports Pub Date : 2025-10-02 DOI: 10.1002/ccr3.70998
Fahad Khalid Soleja, Aamna Mujtaba, Alizeh Imran, Marium Omair Mirza, Mahfuza Anan
{"title":"Osteomyelitis as a Rare Complication in an 8-Year-Old Boy With Beta Thalassemia: A Case Report","authors":"Fahad Khalid Soleja,&nbsp;Aamna Mujtaba,&nbsp;Alizeh Imran,&nbsp;Marium Omair Mirza,&nbsp;Mahfuza Anan","doi":"10.1002/ccr3.70998","DOIUrl":"https://doi.org/10.1002/ccr3.70998","url":null,"abstract":"<p>Osteomyelitis in patients suffering from thalassemia major requires a multidisciplinary approach involving bone debridement, external fixation, and a prolonged course of antibiotics. Amnion grafting, an emerging technique, has demonstrated promising results in accelerating bone healing and enhancing tissue regeneration. Given these encouraging findings, using fresh amnion grafts in osteomyelitis treatment warrants further research to optimize clinical outcomes.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ccr3.70998","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145224111","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
Dentofacial Features in Schimke Immuno-Osseous Dysplasia: From Childhood to Adolescence Schimke免疫-骨发育不良的牙面特征：从儿童期到青春期。
IF 0.6
Clinical Case Reports Pub Date : 2025-10-01 DOI: 10.1002/ccr3.70921
Alireza Sharifinejad, Fateme Parvizi, Maryam Enteghad, Yasamin Ghahramani
{"title":"Dentofacial Features in Schimke Immuno-Osseous Dysplasia: From Childhood to Adolescence","authors":"Alireza Sharifinejad,&nbsp;Fateme Parvizi,&nbsp;Maryam Enteghad,&nbsp;Yasamin Ghahramani","doi":"10.1002/ccr3.70921","DOIUrl":"10.1002/ccr3.70921","url":null,"abstract":"<p>Schimke immune-osseous dysplasia (SIOD) is a sporadic multi-system disorder mainly characterized by spondyloepiphyseal dysplasia, immune insufficiency, and renal failure. Little evidence is available regarding the dentofacial features of SIOD. This study presents the clinical course of a 16-year-old girl suffering from SIOD, focusing on her oral anomalies from her mixed to permanent dentition. After kidney transplantation and immune therapy, the patient discussed herein is supposed to live longer than a majority of the Schimke population. These findings might play a role in the earlier diagnosis of the syndrome and can better emphasize oral care throughout their lives. This is the first study that thoroughly discusses the dental anomalies of an SIOD patient from her mixed to permanent dentition.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12485268/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145212041","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 Eisenmenger Syndrome Presentation in the Intensive Care 重症监护中一种罕见的艾森曼格综合征。
IF 0.6
Clinical Case Reports Pub Date : 2025-10-01 DOI: 10.1002/ccr3.71000
Joana Alves Cabrita, Sérgio Bronze, Bernardo Pereira, Sara Machado, Carlos Pimentel, Sofia Cardoso, Maria João Oliveira, Nuno Germano, Luís Bento
{"title":"A Rare Eisenmenger Syndrome Presentation in the Intensive Care","authors":"Joana Alves Cabrita,&nbsp;Sérgio Bronze,&nbsp;Bernardo Pereira,&nbsp;Sara Machado,&nbsp;Carlos Pimentel,&nbsp;Sofia Cardoso,&nbsp;Maria João Oliveira,&nbsp;Nuno Germano,&nbsp;Luís Bento","doi":"10.1002/ccr3.71000","DOIUrl":"10.1002/ccr3.71000","url":null,"abstract":"<p>This case report gives a lesson about the importance of being aware of subtle signs of cardiorespiratory distress in young patients. It reports an 18-year-old woman in whom a 19 mm ventricular septal defect was detected after a procedure, with acute cardiopulmonary deterioration being managed in the ICU.</p>","PeriodicalId":10327,"journal":{"name":"Clinical Case Reports","volume":"13 10","pages":""},"PeriodicalIF":0.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12485274/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145211931","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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