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Case Reports in Clinical Radiology最新文献

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Atypical demyelinating lesion of corpus callosum mimicking malignant mass lesion 胼胝体非典型脱髓鞘病变，类似恶性肿块病变
Case Reports in Clinical Radiology Pub Date : 2023-08-01 DOI: 10.25259/crcr_111_2023
Bheru Dan Charan, S. Gaikwad, Nikhila Reddy, Ekamjot Singh
{"title":"Atypical demyelinating lesion of corpus callosum mimicking malignant mass lesion","authors":"Bheru Dan Charan, S. Gaikwad, Nikhila Reddy, Ekamjot Singh","doi":"10.25259/crcr_111_2023","DOIUrl":"https://doi.org/10.25259/crcr_111_2023","url":null,"abstract":"Tumefactive demyelination is a demyelinating disease that exhibits clinical and radiologic features similar to those of brain tumors. These lesions present a significant diagnostic challenge. The utilization of magnetic resonance imaging (MRI) imaging can contribute to the preoperative diagnosis of these lesions. In this case report, we highlight the importance of MRI in the diagnosis of tumefactive demyelination.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"292 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131945904","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
Early MR brain findings in a neonate with molybdenum cofactor deficiency 钼辅助因子缺乏症新生儿早期脑磁共振发现
Case Reports in Clinical Radiology Pub Date : 2023-07-29 DOI: 10.25259/crcr_98_2023
Hirva Manek, F. Gala
{"title":"Early MR brain findings in a neonate with molybdenum cofactor deficiency","authors":"Hirva Manek, F. Gala","doi":"10.25259/crcr_98_2023","DOIUrl":"https://doi.org/10.25259/crcr_98_2023","url":null,"abstract":"Molybdenum cofactor deficiency (MoCD) is an inborn error of metabolism which presents with neonatal encephalopathy, seizures, and a turbulent postnatal course. It is an under-recognized cause of neonatal encephalopathy as it mimics hypoxic ischemic encephalopathy (HIE) on imaging. We present the case of an affected male neonate of a twin pregnancy whose magnetic resonance imaging in the early neonatal period showed restricted diffusion in lobar distribution with areas of cystic gliosis and mild tortuosity of the intracranial vessels. There are only a few case reports to the best of our knowledge which describe magnetic resonance (MR) findings of MoCD on diffusion-weighted images, none of which mentions unilateral changes or vessel tortuosity. MoCD should be considered in children with MR findings mimicking HIE in the absence of a history of perinatal hypoxia. This is important as the disorder has a poorer prognosis and the parents need appropriate prenatal counseling.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"77 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127391585","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
Case reports: Equivalent to bedside teaching in new era of social media 案例报告:相当于社交媒体新时代的床边教学
Case Reports in Clinical Radiology Pub Date : 2023-07-26 DOI: 10.25259/crcr_129_2023
B. Sureka
{"title":"Case reports: Equivalent to bedside teaching in new era of social media","authors":"B. Sureka","doi":"10.25259/crcr_129_2023","DOIUrl":"https://doi.org/10.25259/crcr_129_2023","url":null,"abstract":"","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133415558","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
Colo-renal-duodenal fistula in pediatric patient with acute lymphoblastic leukemia: A rare presentation 小儿急性淋巴细胞白血病患者的结肠-肾-十二指肠瘘:罕见的表现
Case Reports in Clinical Radiology Pub Date : 2023-07-24 DOI: 10.25259/crcr_84_2023
Komal Sood, P. Gupta, Aanchal Bhayana, A. Malik
{"title":"Colo-renal-duodenal fistula in pediatric patient with acute lymphoblastic leukemia: A rare presentation","authors":"Komal Sood, P. Gupta, Aanchal Bhayana, A. Malik","doi":"10.25259/crcr_84_2023","DOIUrl":"https://doi.org/10.25259/crcr_84_2023","url":null,"abstract":"Colo-renal fistulas are uncommon presentations in the pediatric population and usually have an underlying insult, which can be vascular, infective, inflammatory, penetrating trauma, tumor, or iatrogenic in postintervention or postoperative procedures. Although few cases of such fistulae are published earlier, there is extreme paucity of literature on colo-renal fistulas in association with acute lymphoblastic leukemia (ALL). A thorough literature search revealed only one similar case report in a 15-year-old patient, to the best of our knowledge. Here, we present another case of a 6-year-old female patient, a known case of T-cell ALL with febrile neutropenia, uncontrolled hypertension, and fever spikes. The patient developed a colo-renal-duodenal fistula subsequent to a vascular and infective insult to the right kidney.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"39 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122648305","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
Unusual case of falciform ligament internal hernia in pregnancy 妊娠镰状韧带内疝的罕见病例
Case Reports in Clinical Radiology Pub Date : 2023-07-24 DOI: 10.25259/crcr_102_2023
S. Rajesh, V. Arunachalam, Swathigha Selvaraj, Pudhiavan Arunachalam, Ganesan Ayyasamy
{"title":"Unusual case of falciform ligament internal hernia in pregnancy","authors":"S. Rajesh, V. Arunachalam, Swathigha Selvaraj, Pudhiavan Arunachalam, Ganesan Ayyasamy","doi":"10.25259/crcr_102_2023","DOIUrl":"https://doi.org/10.25259/crcr_102_2023","url":null,"abstract":"Acute abdomen in pregnancy poses various diagnostic challenges due to limitations in imaging modalities. It can be due to an obstetric or non-obstetric cause. Internal hernia through congenital defects is rare. Although internal hernia is not prevalent in pregnancy, it is increasing nowadays due to previous surgical defects in the mesentery and peritoneal folds. We report an unusual case of an internal hernia through a defect in the falciform ligament in a pregnant female where imaging findings helped in timely surgical intervention.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"60 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121681395","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
“Leopard skin” sign: Magnetic resonance imaging appearance of Lhermitte-Duclos disease with histopathologic correlation “豹皮征”:Lhermitte-Duclos病的磁共振成像表现与组织病理学相关
Case Reports in Clinical Radiology Pub Date : 2023-07-24 DOI: 10.25259/crcr_103_2023
Anitha Mandava, V. Koppula, Suseela Kodandapani, V. Kommu
{"title":"“Leopard skin” sign: Magnetic resonance imaging appearance of Lhermitte-Duclos disease with histopathologic correlation","authors":"Anitha Mandava, V. Koppula, Suseela Kodandapani, V. Kommu","doi":"10.25259/crcr_103_2023","DOIUrl":"https://doi.org/10.25259/crcr_103_2023","url":null,"abstract":"Dysplastic cerebellar gangliocytoma or Lhermitte-Duclos disease (LDD) is a rare hamartomatous malformation of cerebellum that can occur in isolation or as a component of Cowden syndrome. Although uncommon, the characteristic clinical symptoms and magnetic resonance imaging (MRI) features are highly suggestive of the condition and histopathological features confirm the diagnosis. We report a case of LDD, presenting with “Leopard skin” appearance of the lesion on MRI with a brief review of imaging, clinical, and histopathological features.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"243 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131930344","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
The catastrophe of rabies encephalitis: A case series 狂犬病脑炎的灾难:一个病例系列
Case Reports in Clinical Radiology Pub Date : 2023-07-20 DOI: 10.25259/crcr_1_2023
S. Jha, T. Yadav, A. Rohila, Sanjiv Sharma, S. Tiwari
{"title":"The catastrophe of rabies encephalitis: A case series","authors":"S. Jha, T. Yadav, A. Rohila, Sanjiv Sharma, S. Tiwari","doi":"10.25259/crcr_1_2023","DOIUrl":"https://doi.org/10.25259/crcr_1_2023","url":null,"abstract":"Rabies is one of humankind’s oldest and most fatal zoonotic diseases. Few cases of survival post rabies infection have been documented so far. Due to its rapid course of progression, patients succumb before acquiring magnetic resonance imaging (MRI). However, in cases where MRI is feasible, the latter is a valuable source of information that aids in antemortem confirmation of diagnosis when backed by clinical data. We present two cases of rabies encephalitis, with classic imaging features on MRI. Symmetrical involvement of the basal ganglia, mesial temporal lobes, and dorsal portion of the brainstem should raise a suspicion of rabies encephalitis in the proper clinical situation.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"94 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130988926","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
An intriguing case of acute abdomen secondary to ruptured pyomyoma: A case report 子宫肌瘤破裂继发急性腹部1例
Case Reports in Clinical Radiology Pub Date : 2023-06-24 DOI: 10.25259/crcr_88_2023
Greta Vincent, V. Sudheer, A. Varghese, G. Joseph
{"title":"An intriguing case of acute abdomen secondary to ruptured pyomyoma: A case report","authors":"Greta Vincent, V. Sudheer, A. Varghese, G. Joseph","doi":"10.25259/crcr_88_2023","DOIUrl":"https://doi.org/10.25259/crcr_88_2023","url":null,"abstract":"Pyomyoma by definition is a suppurative leiomyoma, as a result of infection of infarcted leiomyoma. Pyomyoma is a gynecological emergency as it can further lead to sepsis and peritonitis resulting in high morbidity and mortality. A high index of clinical suspicion is crucial in the diagnosis, and prompt treatment in the initial stage is recommended to reduce mortality. Ultrasound, computed tomography, and magnetic resonance provide diagnostic clues. We present a case of a 44-year-old woman who presented with an acute abdomen due to a spontaneous rupture of pyomyoma. The patient was treated with total abdominal hysterectomy and salpingooophorectomy along with peritoneal irrigation and drainage.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"44 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116413269","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 rare case of a huge diffuse-type tenosynovial giant cell tumor in the ankle 一例罕见的踝关节巨大弥漫性腱鞘巨细胞瘤
Case Reports in Clinical Radiology Pub Date : 2023-06-24 DOI: 10.25259/crcr_101_2023
Riya Samanta, N. Batta, Abhinetri K. S. V.
{"title":"A rare case of a huge diffuse-type tenosynovial giant cell tumor in the ankle","authors":"Riya Samanta, N. Batta, Abhinetri K. S. V.","doi":"10.25259/crcr_101_2023","DOIUrl":"https://doi.org/10.25259/crcr_101_2023","url":null,"abstract":"Tenosynovial giant cell tumor (TSGCT) is a rare tumor originating from the synovial lining of joints, tendon sheaths, and bursae. It is categorized into localized and diffuse types. The diffuse-type TSGCT (D-TSGCT), formerly called pigmented villonodular synovitis, although benign, can be locally aggressive. Magnetic resonance imaging is the modality of choice for diagnosing and assessing the severity of the disease. The lesions demonstrate characteristic “blooming” on gradient echo sequences. Histopathology reveals villous, nodular, or villonodular components and hemosiderin deposition. Here, we report the case of a 28-year-old man with a huge D-TSGCT in the left ankle.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"110 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125228915","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
An unusual manifestation of neurofibromatosis – A case report of a vulval mass 神经纤维瘤病的一种不寻常表现-外阴肿块1例报告
Case Reports in Clinical Radiology Pub Date : 2023-06-20 DOI: 10.25259/crcr_54_2023
Shivraj M. Ingole, Ayantika Maity
{"title":"An unusual manifestation of neurofibromatosis – A case report of a vulval mass","authors":"Shivraj M. Ingole, Ayantika Maity","doi":"10.25259/crcr_54_2023","DOIUrl":"https://doi.org/10.25259/crcr_54_2023","url":null,"abstract":"Neurofibromatosis (NF) of the female genitalia is an uncommon manifestation. Selective involvement of the labium majus is quite rare. We describe a rare manifestation of a vulval plexiform neurofibroma without clitoral involvement in a post-pubertal girl. The patient had multiple café-au-lait spots over the neck, back, buttocks and thighs, a patch of pigmentation over the pelvis and inguinal region, axillary freckling, and a large hanging left vulval mass. On ultrasound, it showed hypoechoic nodules on a hyperechoic background with significant vascularity. Magnetic resonance imaging revealed T1-weighted (T1W) hypointense and T2-weighted (T2W) hyperintense, diffuse infiltrating lesion with few T2W hyperintense tubular and nodular areas, presence of “target sign,” and intense post-contrast enhancement. A biopsy confirmed it to be neurofibroma. The patient was diagnosed with NF type 1 and underwent surgical resection.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"65 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126442521","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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