Male patient, 20 years old, electrician. No significant personal or family medical history. No regular medication, no known drug allergies. Seeks consultation due to the appearance of a lesion on the posterior side of the neck with 3 months of progression
{"title":"A case of an exuberant skin ring","authors":"Ines ML Terra","doi":"10.52768/2766-7820/2501","DOIUrl":"https://doi.org/10.52768/2766-7820/2501","url":null,"abstract":"Male patient, 20 years old, electrician. No significant personal or family medical history. No regular medication, no known drug allergies. Seeks consultation due to the appearance of a lesion on the posterior side of the neck with 3 months of progression","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139358505","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}
A 12-year-old female patient came to our outpatient department with complaints of low vision in both eyes since childhood. There was no significant history of ocular trauma or family history of similar disease.
{"title":"Microphthalmos with elongated ciliary processes","authors":"Sarath S","doi":"10.52768/2766-7820/2502","DOIUrl":"https://doi.org/10.52768/2766-7820/2502","url":null,"abstract":"A 12-year-old female patient came to our outpatient department with complaints of low vision in both eyes since childhood. There was no significant history of ocular trauma or family history of similar disease.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"130 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139358539","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}
Obturator hernia is a rare disease that affects thin, elderly women. Non-incarcerated hernias are often particularly difficult to diagnose. We present a case of a non-incarcerated obturator hernia diagnosed based on patient history and Computed Tomography (CT) findings.
{"title":"A diagnostically challenging case of non-incarcerated obturator hernia: History and CT findings","authors":"Seiji Yamashiro","doi":"10.52768/2766-7820/2500","DOIUrl":"https://doi.org/10.52768/2766-7820/2500","url":null,"abstract":"Obturator hernia is a rare disease that affects thin, elderly women. Non-incarcerated hernias are often particularly difficult to diagnose. We present a case of a non-incarcerated obturator hernia diagnosed based on patient history and Computed Tomography (CT) findings.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139359515","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}
A 47-year-old female with a documented history of allergies to medicine ingested a 1 gram tablet of amoxicillin for supposed dental pain. After 10 minutes, she began experiencing tongue swelling, throat congestion, shortness of breath, and eventually faints.
{"title":"Transmural colon necrosis induced by amoxicillin anaphylactic shock","authors":"Radu Moldovan","doi":"10.52768/2766-7820/2499","DOIUrl":"https://doi.org/10.52768/2766-7820/2499","url":null,"abstract":"A 47-year-old female with a documented history of allergies to medicine ingested a 1 gram tablet of amoxicillin for supposed dental pain. After 10 minutes, she began experiencing tongue swelling, throat congestion, shortness of breath, and eventually faints.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139359552","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}
A 73-year-old male was admitted to the neurology department complaining of right hemiparesis lasting for 19 hours. At admission, Magnetic Resonance Imaging (MRI) showed acute ischemia in the left cerebral hemisphere, but brain MR angiography and ultrasonography of the carotid artery were unremarkable.
{"title":"Recurrent ischemic stroke due to internal carotid artery dissection","authors":"Jing Zheng","doi":"10.52768/2766-7820/2498","DOIUrl":"https://doi.org/10.52768/2766-7820/2498","url":null,"abstract":"A 73-year-old male was admitted to the neurology department complaining of right hemiparesis lasting for 19 hours. At admission, Magnetic Resonance Imaging (MRI) showed acute ischemia in the left cerebral hemisphere, but brain MR angiography and ultrasonography of the carotid artery were unremarkable.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139359822","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}
A man in his mid-forties presented with a two-day history of sudden onset right upper quadrant pain and coffee-ground vomiting. Eight months previously, he underwent successful endoscopic retrograde cholangiopancreatography (ERCP) with biliary stenting for cholangitis and severe gallstone pancreatitis. This was followed by a COVID-delayed uncomplicated laparoscopic cholecystectomy.
{"title":"Blood and bile: A gastroduodenal artery pseudoaneurysm associated with endoscopic retrograde cholangiopancreatography stent migration","authors":"Prashanth Ramaraj","doi":"10.52768/2766-7820/2497","DOIUrl":"https://doi.org/10.52768/2766-7820/2497","url":null,"abstract":"A man in his mid-forties presented with a two-day history of sudden onset right upper quadrant pain and coffee-ground vomiting. Eight months previously, he underwent successful endoscopic retrograde cholangiopancreatography (ERCP) with biliary stenting for cholangitis and severe gallstone pancreatitis. This was followed by a COVID-delayed uncomplicated laparoscopic cholecystectomy.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"299 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139359689","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}
Arterial Tortuosity Syndrome (ATS) is a very rare autosomal recessive disorder, that affects the connective tissue. The incidence of ATS is not well known and to date only 106 patients have been described in literature. ATS affects medium and large sizes arteries, leading to a widespread elongation and to an intensification of the average vessel tortuousness, responsible of several loops and kinks.
{"title":"Imaging in a rare case of neonatal arterial tortuosity syndrome","authors":"Maria Cristina Inserra","doi":"10.52768/2766-7820/2496","DOIUrl":"https://doi.org/10.52768/2766-7820/2496","url":null,"abstract":"Arterial Tortuosity Syndrome (ATS) is a very rare autosomal recessive disorder, that affects the connective tissue. The incidence of ATS is not well known and to date only 106 patients have been described in literature. ATS affects medium and large sizes arteries, leading to a widespread elongation and to an intensification of the average vessel tortuousness, responsible of several loops and kinks.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139360234","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}
A middle-aged female presented with vague abdominal symptoms that after diagnostic and staging work up was revealed to be an advanced case of combined hepatocellular and cholangiocarcinoma (cHCC-CCA). She was started on systemic chemotherapy inspite of which experienced disease progression
{"title":"Combined hepatocellular and cholangiocarcinoma: A rare pathological diagnosis, clinically mimicking its parent phenotypes","authors":"Indra Jeet Gupta","doi":"10.52768/2766-7820/2495","DOIUrl":"https://doi.org/10.52768/2766-7820/2495","url":null,"abstract":"A middle-aged female presented with vague abdominal symptoms that after diagnostic and staging work up was revealed to be an advanced case of combined hepatocellular and cholangiocarcinoma (cHCC-CCA). She was started on systemic chemotherapy inspite of which experienced disease progression","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139360220","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}
Cervical Vertigo is a controversial entity. Here we present an un reported case of Isolated Atlanto Occipital Joint effusion as a cause of Vertigo. A 45-year-old male presented with imbalance, ataxia, swaying, quick spins, and oscillopsia, especially when turning his head.
{"title":"Isolated atlanto-occipital joint effusion presenting as cervicogenic vertigo","authors":"Dr. Sandeep Kumar","doi":"10.52768/2766-7820/2494","DOIUrl":"https://doi.org/10.52768/2766-7820/2494","url":null,"abstract":"Cervical Vertigo is a controversial entity. Here we present an un reported case of Isolated Atlanto Occipital Joint effusion as a cause of Vertigo. A 45-year-old male presented with imbalance, ataxia, swaying, quick spins, and oscillopsia, especially when turning his head.","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"193 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139360365","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}
The gut microbiota can influence the brain function through a variety of ways, but its role in the etiology of Bipolar Disorder (BD) is yet unknown. The brain and the gut are linked through a communication pathway called the Microbiota-Gut-Brain Axis (MGBA).
{"title":"Linking the gut microbiota to brain dysfunction in bipolar disorder: Evidence from neuroimaging","authors":"H. Md","doi":"10.52768/2766-7820/2493","DOIUrl":"https://doi.org/10.52768/2766-7820/2493","url":null,"abstract":"The gut microbiota can influence the brain function through a variety of ways, but its role in the etiology of Bipolar Disorder (BD) is yet unknown. The brain and the gut are linked through a communication pathway called the Microbiota-Gut-Brain Axis (MGBA).","PeriodicalId":15420,"journal":{"name":"Journal of Clinical Images and Medical Case Reports","volume":"41 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139360502","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}
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