Elevated homocysteine level in serum or hyperhomocysteinemia is considered to be closely associated with neurological disorders such as stroke and cardiovascular diseases. However, to date, there have been limited studies on symptoms specifically associated with elevated homocysteine levels
{"title":"Early symptoms and signs of bony and brain lesions associated with hyperhomocysteinemia: Evidence with scintigraphic images of skeleton and brain","authors":"Shin-Tsu Chang","doi":"10.52768/2833-2725/1140","DOIUrl":"https://doi.org/10.52768/2833-2725/1140","url":null,"abstract":"Elevated homocysteine level in serum or hyperhomocysteinemia is considered to be closely associated with neurological disorders such as stroke and cardiovascular diseases. However, to date, there have been limited studies on symptoms specifically associated with elevated homocysteine levels","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"7 5","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135219009","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}
Hemorrhagic cholecystitis is a very rare condition. It can present very different clinical symptoms. It often occurs as a complication of cholecystitis. These patients are usually under anticoagulant therapy or they have coagulopathy.
{"title":"Hemorrhagic cholecystitis causing an intrahepatic subcapsular hematoma: Case report and review of the literature","authors":"Yunus Sur","doi":"10.52768/2833-2725/1139","DOIUrl":"https://doi.org/10.52768/2833-2725/1139","url":null,"abstract":"Hemorrhagic cholecystitis is a very rare condition. It can present very different clinical symptoms. It often occurs as a complication of cholecystitis. These patients are usually under anticoagulant therapy or they have coagulopathy.","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"36 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134903862","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}
Megalencephalic Leucoencephalopathy with subcortical Cysts (MLC) is a rare autosomal recessive disease with onset in infancy. Typically, the first symptom is macrocephaly which becomes evident in the first year of life [1-3].
{"title":"Megalencephalic leucoencephalopathy with subcortical cysts: A cause of early seizures after trivial head trauma","authors":"Elena Pasini","doi":"10.52768/2833-2725/1138","DOIUrl":"https://doi.org/10.52768/2833-2725/1138","url":null,"abstract":"Megalencephalic Leucoencephalopathy with subcortical Cysts (MLC) is a rare autosomal recessive disease with onset in infancy. Typically, the first symptom is macrocephaly which becomes evident in the first year of life [1-3].","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"161 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135110202","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- years-old man was referred to emergency department with bilateral flank pain and new-onset hematuria. He had a history of prostatic cancer and recurrent urinary tract infections
一名73岁男性病患因双侧腹部疼痛及新发血尿被转介至急诊科。他有前列腺癌和复发性尿路感染的病史
{"title":"Bladder jackstone induced by prostate cancer","authors":"Mohamad Zbidat","doi":"10.52768/2833-2725/1137","DOIUrl":"https://doi.org/10.52768/2833-2725/1137","url":null,"abstract":"A 73- years-old man was referred to emergency department with bilateral flank pain and new-onset hematuria. He had a history of prostatic cancer and recurrent urinary tract infections","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135487017","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}
Hydralazine-induced anti-neutrophil cytoplasmic antibody vasculitis may occur any time after hydralazine initiation. General internists should recognize diffuse alveolar hemorrhage as a rare complication of this condition, as early treatment reduces the associated high risk of mortality.
{"title":"A rare case of hydralazine-induced diffuse alveolar hemorrhage","authors":"Evan Raf","doi":"10.52768/2833-2725/1136","DOIUrl":"https://doi.org/10.52768/2833-2725/1136","url":null,"abstract":"Hydralazine-induced anti-neutrophil cytoplasmic antibody vasculitis may occur any time after hydralazine initiation. General internists should recognize diffuse alveolar hemorrhage as a rare complication of this condition, as early treatment reduces the associated high risk of mortality.","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135787542","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}
We present a case of a 12-year-old patient suffering from progressive spastic paraparesis secondary to multiple contrastenhancing ependymal spinal cord lesions
我们提出了一个12岁的病人患有继发于多发性增强对比室管膜脊髓病变的进行性痉挛性截瘫
{"title":"Neurosarcoidosis leading to a rosary-like pattern","authors":"Patricia Alejandra Garrido Ruiz","doi":"10.52768/2833-2725/1135","DOIUrl":"https://doi.org/10.52768/2833-2725/1135","url":null,"abstract":"We present a case of a 12-year-old patient suffering from progressive spastic paraparesis secondary to multiple contrastenhancing ependymal spinal cord lesions","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136364376","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}
Introduction: Petrous Bone Cholesteatomas (PBCs) are epidermoid cysts, which have developed in the petrous portion of the temporal bone and may be congenital or acquired.
石质骨胆脂瘤(pbc)是发生在颞骨石质部分的表皮样囊肿，可能是先天性的或后天的。
{"title":"Cholesteatoma of petrous bone: Auditory improvement with surgical treatment novel application of the posterior retrosigmoid approach","authors":"Alejandra Arevalo-Saenz","doi":"10.52768/2833-2725/1134","DOIUrl":"https://doi.org/10.52768/2833-2725/1134","url":null,"abstract":"Introduction: Petrous Bone Cholesteatomas (PBCs) are epidermoid cysts, which have developed in the petrous portion of the temporal bone and may be congenital or acquired.","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"51 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135369622","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 29-year-old pregnant woman was referred to our hospital at the gestational age of 15 weeks. The umbilical cord hernia was pointed out during a fetal echocardiogram at the previous obstetrician’s office, and the patient was referred to our obstetrician
{"title":"Body stalk anomaly","authors":"Kentaro Okamoto","doi":"10.52768/2833-2725/1133","DOIUrl":"https://doi.org/10.52768/2833-2725/1133","url":null,"abstract":"A 29-year-old pregnant woman was referred to our hospital at the gestational age of 15 weeks. The umbilical cord hernia was pointed out during a fetal echocardiogram at the previous obstetrician’s office, and the patient was referred to our obstetrician","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"38 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136036225","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}
Familial Hypercholesterolemia (FH) is a disease with a homozygous or heterozygous autosomal dominant inheritance pattern. It is characterized by high plasma concentrations of Low-Density Lipoprotein (LDL) cholesterol
{"title":"Importance of the detection of genetic diseases associated with cardiovascular risk in pediatric age","authors":"Juan Manuel Sanchez Vargas","doi":"10.52768/2833-2725/1132","DOIUrl":"https://doi.org/10.52768/2833-2725/1132","url":null,"abstract":"Familial Hypercholesterolemia (FH) is a disease with a homozygous or heterozygous autosomal dominant inheritance pattern. It is characterized by high plasma concentrations of Low-Density Lipoprotein (LDL) cholesterol","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"157 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134983500","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}
Lymphangioleiomyomatosis (LAM) is a rare disorder involving young female patients. We present a 35 years old female who presented to the emergency room for abdominal pain due to ureteral stone
{"title":"Asymptomatic presentation of a rare disease: Lymphangioleiomyomatosis","authors":"Som N Chalise","doi":"10.52768/2833-2725/1131","DOIUrl":"https://doi.org/10.52768/2833-2725/1131","url":null,"abstract":"Lymphangioleiomyomatosis (LAM) is a rare disorder involving young female patients. We present a 35 years old female who presented to the emergency room for abdominal pain due to ureteral stone","PeriodicalId":108891,"journal":{"name":"Open Journal of Clinical and Medical Images","volume":"29 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136214589","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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