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Case Reports in Clinical Radiology最新文献

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Imaging findings of cerebral fat embolism 脑脂肪栓塞的影像学表现
Case Reports in Clinical Radiology Pub Date : 2023-06-20 DOI: 10.25259/crcr_79_2023
Mohammed Shakeebuddin Kashif, Vinay Martin Dsa Prabhu, Anand Kalegowda, U. Krishnamurthy
{"title":"Imaging findings of cerebral fat embolism","authors":"Mohammed Shakeebuddin Kashif, Vinay Martin Dsa Prabhu, Anand Kalegowda, U. Krishnamurthy","doi":"10.25259/crcr_79_2023","DOIUrl":"https://doi.org/10.25259/crcr_79_2023","url":null,"abstract":"Cerebral fat embolism (CFE) is a rare complication of long bone or pelvic fractures. The diagnosis is difficult because of non-specific signs and symptoms occurring in conjunction with the features of traumatic injury, where imaging is often deferred in view of unstable vitals. We present two cases of CFE occurring post-internal fixation of femur fracture in young- and middle-aged adult males in early and late subacute stages, respectively; one patient had associated hypoxic-ischemic encephalopathy. It is important for radiologists to know the variable appearance on imaging to make a timely diagnosis.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"19 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":"127793716","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
Unusually large craniopharyngioma: A case report 异常大的颅咽管瘤1例
Case Reports in Clinical Radiology Pub Date : 2023-06-13 DOI: 10.25259/crcr_52_2023
M. Karmakar, Debashis Dakshit, S. Saha, Arnab Bose
{"title":"Unusually large craniopharyngioma: A case report","authors":"M. Karmakar, Debashis Dakshit, S. Saha, Arnab Bose","doi":"10.25259/crcr_52_2023","DOIUrl":"https://doi.org/10.25259/crcr_52_2023","url":null,"abstract":"\u0000\u0000Craniopharyngiomas are benign slow-growing tumors of the central nervous system originating from squamous remnants of incompletely involuted craniopharyngeal duct. Craniopharyngiomas are said to be “giant” when they attain sizes of 5–6 cm or more.\u0000\u0000\u0000\u0000Here, we present a case of unusually large craniopharyngioma in a child, which, to the best of our knowledge, is the largest craniopharyngioma reported in the literature. The provisional diagnosis of craniopharyngioma was established using computed tomography and magnetic resonance imaging.\u0000\u0000\u0000\u0000Craniopharyngiomas are to be considered in the differentials for sellar and suprasellar region lesions causing mass effect. The provisional diagnosis is established by imaging but definitive diagnosis always requires histopathology.\u0000","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"38 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124324596","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
Two rare cases of idiopathic spontaneous extra-axial spinal hematoma 特发性自发性轴外脊髓血肿2例
Case Reports in Clinical Radiology Pub Date : 2023-06-07 DOI: 10.25259/crcr_81_2023
S. Jayanthan, G. Rupesh, Packia Agnes Vimalan, K. Nadanasadharam
{"title":"Two rare cases of idiopathic spontaneous extra-axial spinal hematoma","authors":"S. Jayanthan, G. Rupesh, Packia Agnes Vimalan, K. Nadanasadharam","doi":"10.25259/crcr_81_2023","DOIUrl":"https://doi.org/10.25259/crcr_81_2023","url":null,"abstract":"Spinal hematoma is a rare condition but can cause significant spinal injury and resultant morbidity. Magnetic resonance imaging (MRI) is the gold standard of radiological investigation and is often an emergency indication for imaging. Early diagnosis is crucial for treatment and better patient outcome. Herein, we report two cases of rare idiopathic spontaneous extra-axial hematoma highlighting the role of MRI in the diagnosis.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"36 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126448908","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
Disseminated uterine actinomycosis: Case report and review of literature 弥散性子宫放线菌病1例报告及文献复习
Case Reports in Clinical Radiology Pub Date : 2023-06-07 DOI: 10.25259/crcr_77_2023
N. Ghonge, Surabhi Gupta, Sarika Gupta, Seema Singhal
{"title":"Disseminated uterine actinomycosis: Case report and review of literature","authors":"N. Ghonge, Surabhi Gupta, Sarika Gupta, Seema Singhal","doi":"10.25259/crcr_77_2023","DOIUrl":"https://doi.org/10.25259/crcr_77_2023","url":null,"abstract":"Actinomyces - It mainly affects the cervicofacial and abdominopelvic organs. These bacteria are of low virulence and their spread requires breakdown or alteration of the normal tissue barrier, which can be due to any surgery, trauma, or infection. Actinomyces infection involving the reproductive organs may often mimic a neoplasm and lead to aggressive surgical management for the patient; it is therefore necessary to recognize the infection which can be effectively managed using a combination of pharmaceutical agents. Imaging such as computed tomography and magnetic resonance imaging aid in determining the extent of the disease. Histopathological diagnosis/culture is necessary to make the final diagnosis. We present a case of actinomycosis of the uterus manifesting as a large uterine mass with dissemination to the pelvis and anterior abdominal wall.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125958873","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
Atypical presentation of a cystic parathyroid adenoma: Acute airway compromise secondary to intratumoral apoplexy - A case report 囊性甲状旁腺腺瘤的不典型表现:急性气道损害继发于瘤内中风- 1例报告
Case Reports in Clinical Radiology Pub Date : 2023-06-07 DOI: 10.25259/crcr_41_2023
Pravitha Baskar, S. Rajasekaran, Swathigha Selvaraj, V. Arunachalam, P. S. Shobhanaa
{"title":"Atypical presentation of a cystic parathyroid adenoma: Acute airway compromise secondary to intratumoral apoplexy - A case report","authors":"Pravitha Baskar, S. Rajasekaran, Swathigha Selvaraj, V. Arunachalam, P. S. Shobhanaa","doi":"10.25259/crcr_41_2023","DOIUrl":"https://doi.org/10.25259/crcr_41_2023","url":null,"abstract":"Spontaneous hemorrhage into cystic parathyroid lesion is a very rare and life-threatening complication which poses diagnostic challenge to the clinician as well as the radiologist due to various close mimics. Prompt identification, diagnosis, and emergent treatment are imperative to save the life of the patient. We report a case of a 56-year-old female who presented with acute airway compromise due to a giant cystic parathyroid adenoma with spontaneous hemorrhage. Magnetic resonance imaging was performed, and the patient underwent surgical exploration.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"3 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114306984","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 small bowel gangrene and perforation following high voltage electrical injury 高压电伤致小肠坏疽穿孔一例
Case Reports in Clinical Radiology Pub Date : 2023-06-03 DOI: 10.25259/crcr_8_2023
M. Reddy, Rajani Gorantla, Mallikarjuna Reddy Mandapati
{"title":"A rare case of small bowel gangrene and perforation following high voltage electrical injury","authors":"M. Reddy, Rajani Gorantla, Mallikarjuna Reddy Mandapati","doi":"10.25259/crcr_8_2023","DOIUrl":"https://doi.org/10.25259/crcr_8_2023","url":null,"abstract":"This case is a 42-year-old male with an alleged history of electric shock. About 8 h after the insult, an ulcer in the right iliac fossa increased in size with fecal matter coming out. Contrast-enhanced computed tomography of the abdomen revealed a full thickness anterior abdominal wall defect with prolapse of a segment of the distal ileal loop, showing discontinuous wall and no wall enhancement suggestive of evisceration and perforation of bowel with gangrene.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"109 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124757094","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
Imaging in sacrococcygeal subcutaneous myxopapillary ependymoma: Sporadically reported from Asian population 骶尾骨皮下黏液乳头状室管膜瘤的影像学表现:亚洲人群的零星报道
Case Reports in Clinical Radiology Pub Date : 2023-06-03 DOI: 10.25259/crcr_74_2023
C. Dhandhalya, S. Chudasama, Hiral Kishorbhai Pansuriya
{"title":"Imaging in sacrococcygeal subcutaneous myxopapillary ependymoma: Sporadically reported from Asian population","authors":"C. Dhandhalya, S. Chudasama, Hiral Kishorbhai Pansuriya","doi":"10.25259/crcr_74_2023","DOIUrl":"https://doi.org/10.25259/crcr_74_2023","url":null,"abstract":"Subcutaneous myxopapillary ependymoma in sacrococcygeal region is an unusual neoplasm. It usually affects younger age groups. Only sporadic case reports from the Asian population have been reported. We here report a case of subcutaneous sacrococcygeal myxopapillary ependymoma suspected at ultrasound, suggested at magnetic resonance imaging examination, and confirmed histologically in a 10-year-old boy. We aimed at explaining its pathology, clinical implications, management, and relevant literature review.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125462339","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
Disseminated langerhans cell histiocytosis presenting as decompensated childhood cirrhosis 弥散性朗格汉斯细胞组织细胞增多症表现为失代偿性儿童肝硬化
Case Reports in Clinical Radiology Pub Date : 2023-05-31 DOI: 10.25259/crcr_46_2023
Khushboo Tekriwal, A. Bhoir, P. Badhe, Zilliani Alam
{"title":"Disseminated langerhans cell histiocytosis presenting as decompensated childhood cirrhosis","authors":"Khushboo Tekriwal, A. Bhoir, P. Badhe, Zilliani Alam","doi":"10.25259/crcr_46_2023","DOIUrl":"https://doi.org/10.25259/crcr_46_2023","url":null,"abstract":"Childhood cirrhosis is a rare disease of multifactorial etiopathogenesis. One of the rare underlying causes is Langerhans cell histiocytosis (LCH). The multifocal multisystemic variant of LCH can rarely involve the hepatobiliary system. Indirect and direct forms of hepatobiliary involvement are known. Early diagnosis of underlying liver involvement in cases of LCH is crucial to prevent decompensation and ameliorate prognosis post-liver transplantation. This is a case of an 18-month-old male child who developed cutaneous lesions in the early infancy. He was brought to clinical attention due to progressively increasing abdominal girth. His laboratory, clinical and radiological examination suggested multisystem pathology, subsequently confirmed on biopsy as LCH with predominant involvement of hepatobiliary, pulmonary, and integumentary systems. Unfortunately, he succumbed within a week of diagnosis.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115294320","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
Situs ambiguous-polysplenia syndrome: Torsion splenunculus – A rare cause of acute abdomen pain 位置模糊-多脾综合征:脾扭转-急性腹痛的罕见原因
Case Reports in Clinical Radiology Pub Date : 2023-05-31 DOI: 10.25259/crcr_64_2023
S. Jayanthan, T. Moorthy, N. Karunakaran, K. Nadanasadharam
{"title":"Situs ambiguous-polysplenia syndrome: Torsion splenunculus – A rare cause of acute abdomen pain","authors":"S. Jayanthan, T. Moorthy, N. Karunakaran, K. Nadanasadharam","doi":"10.25259/crcr_64_2023","DOIUrl":"https://doi.org/10.25259/crcr_64_2023","url":null,"abstract":"Situs ambiguous, also known as heterotaxy syndrome, is a rare congenital condition in which there is an abnormal positioning of internal organs of the chest and abdomen. Polysplenia (left isomerism) is a common association with it and hence called as “Situs Ambiguous-Polysplenia” syndrome. Torsion splenunculi is a rare complication associated with it. Herein, we report a case of splenunculi torsion in an adult with situs ambiguous associated with polysplenia.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"28 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121511776","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 unique case of agenesis of corpus callosum with concomitant midline teratoma and dorsal interhemispheric cyst 胼胝体发育不全伴中线畸胎瘤和背半球间囊肿的独特病例
Case Reports in Clinical Radiology Pub Date : 2023-05-29 DOI: 10.25259/crcr_32_2023
Namrata Bagchi, Jyoti Gupta, Bhanukiran Chauhan, Rupi Jamwal
{"title":"A unique case of agenesis of corpus callosum with concomitant midline teratoma and dorsal interhemispheric cyst","authors":"Namrata Bagchi, Jyoti Gupta, Bhanukiran Chauhan, Rupi Jamwal","doi":"10.25259/crcr_32_2023","DOIUrl":"https://doi.org/10.25259/crcr_32_2023","url":null,"abstract":"Midline interhemispheric cyst with corpus callosal agenesis is a well recognized condition and has been associated with various genetic conditions. Associated extraaxial tumors are uncommon with no proven genetic association. We describe a rare case of corpus callosal agenesis with a dorsal interhemispheric cyst and an extraaxial teratoma in the basifrontal region and review its imaging features along with the etiopathogenesis of concurrence of such condition.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"10 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133214366","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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