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Case Reports in Clinical Radiology最新文献

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Unusual presentation of subcapsular renal pseudocyst as page kidney – A case report 肾包膜下假性囊肿异常表现为页肾1例
Case Reports in Clinical Radiology Pub Date : 2023-04-12 DOI: 10.25259/crcr_38_2023
S. Thakur, Sumala Kapila, S. Makhaik, A. Jhobta
{"title":"Unusual presentation of subcapsular renal pseudocyst as page kidney – A case report","authors":"S. Thakur, Sumala Kapila, S. Makhaik, A. Jhobta","doi":"10.25259/crcr_38_2023","DOIUrl":"https://doi.org/10.25259/crcr_38_2023","url":null,"abstract":"Page kidney is a rare but potentially curable cause of secondary hypertension. While the pancreatic pseudocyst is a completely different and unrelated entity. Here, we report a case of a 45-year-old female, diagnosed with idiopathic acute pancreatitis with multiple pseudocysts. After successful ultrasound -guided drainage of her left subcapsular renal pseudocyst, she became normotensive again, confirming the diagnosis of page kidney. This case highlights dual reasons that prompted us to report the case. The first being such remotely located subcapsular renal pseudocyst as itself a rare entity and the second, its unusual presentation as page kidney. The case emphasizes on the early management of such patients so as to salvage renal function.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"8 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127487256","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
Tricuspid valve metastasis in osteosarcoma, paving way through iliofemoral vessels – An unusual presentation of a usual diagnosis 骨肉瘤中三尖瓣转移，通过髂股血管铺平道路-一种不寻常的诊断表现
Case Reports in Clinical Radiology Pub Date : 2023-04-10 DOI: 10.25259/crcr_31_2023
{"title":"Tricuspid valve metastasis in osteosarcoma, paving way through iliofemoral vessels – An unusual presentation of a usual diagnosis","authors":"","doi":"10.25259/crcr_31_2023","DOIUrl":"https://doi.org/10.25259/crcr_31_2023","url":null,"abstract":"Hematogenous spread of osteosarcoma is a common knowledge, with frequent metastases to lungs and bones. Cardiac involvement is rare finding, most of them depicting contiguous cardiac extension through vessels into the right atrium. Tricuspid metastases are rare. We encountered one such rare case of femur osteosarcoma with multiorgan metastasis including systemic veins, cardiac chambers, and tricuspid valve involvement which presented as diagnostic dilemma. Early detection was crucial for further management and prognostication of patient.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115280148","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
Spontaneous regression of biologically aggressive breast carcinoma: A case report 生物侵袭性乳腺癌自发性消退1例
Case Reports in Clinical Radiology Pub Date : 2023-04-05 DOI: 10.25259/crcr_5_2023
{"title":"Spontaneous regression of biologically aggressive breast carcinoma: A case report","authors":"","doi":"10.25259/crcr_5_2023","DOIUrl":"https://doi.org/10.25259/crcr_5_2023","url":null,"abstract":"The spontaneous regression of cancer is the partial or complete remission of a tumor without treatment, and this has been linked to trauma and infection. The present case details the rare spontaneous regression of a triple negative Grade III ductal carcinoma in the breast. The findings suggest that in our case, this may have been triggered by biopsy and marker clip deployment, and it highlights the importance of being aware of this unusual occurrence so timely diagnosis can be made without causing undue anxiety in patients.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"42 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125506261","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
Bulging ovaries and uterus – A rare case of the canal of Nuck hernia 卵巢、子宫膨出-颈管疝1例
Case Reports in Clinical Radiology Pub Date : 2023-04-05 DOI: 10.25259/crcr_20_2023
P. Sherwani, Saurya Saurya, G. Sharma
{"title":"Bulging ovaries and uterus – A rare case of the canal of Nuck hernia","authors":"P. Sherwani, Saurya Saurya, G. Sharma","doi":"10.25259/crcr_20_2023","DOIUrl":"https://doi.org/10.25259/crcr_20_2023","url":null,"abstract":"Embryologically, patent processus vaginalis in females may present with a canal of Nuck hernia with herniation of the bowel, omentum, or rarely uterus and bilateral ovaries into the inguinal canal and labia. There may be complications like torsion of the herniated ovaries. Precise and early diagnosis of the entity on high-resolution ultrasonography will help in early diagnosis and prevention of complications. Here, we describe a rare case of the canal of Nuck hernia with herniation of the uterus and bilateral ovaries in a 5-month-old female.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"237 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123202396","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 mononeuropathy in child: Intraneural perineurioma of sciatic nerve 儿童单一神经病变罕见病例:坐骨神经神经内神经周围瘤
Case Reports in Clinical Radiology Pub Date : 2023-04-05 DOI: 10.25259/crcr_21_2023
Abhijeet Taori, D. Malpani
{"title":"Unusual case of mononeuropathy in child: Intraneural perineurioma of sciatic nerve","authors":"Abhijeet Taori, D. Malpani","doi":"10.25259/crcr_21_2023","DOIUrl":"https://doi.org/10.25259/crcr_21_2023","url":null,"abstract":"Intraneural perineurioma is a benign nerve sheath tumor of the perineurium characterized by focal perineural cell proliferation. It is primarily seen in young adults. Early childhood presentation is uncommon. We present this interesting case in a child with overall clinical assessment, nerve conduction tests, and magnetic resonance findings in keeping with intraneural perineurioma of the sciatic nerve. It is essential to recognize this potentially treatable disease entity in the early childhood and exclude other causes of nerve palsy.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"386 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122849116","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
Diffusion tensor imaging in evaluation of intradural spinal tumors – A case series 弥散张量成像在脊髓硬膜内肿瘤评估中的应用-一个病例系列
Case Reports in Clinical Radiology Pub Date : 2023-03-13 DOI: 10.25259/crcr_56_2022
Suryansh Arora, Shibani Mehra, U. Garga
{"title":"Diffusion tensor imaging in evaluation of intradural spinal tumors – A case series","authors":"Suryansh Arora, Shibani Mehra, U. Garga","doi":"10.25259/crcr_56_2022","DOIUrl":"https://doi.org/10.25259/crcr_56_2022","url":null,"abstract":"Diffusion tensor imaging (DTI) is an advanced magnetic resonance imaging (MRI) technique which utilizes diffusion measurements in multiple directions to provide information regarding tissue structure by parameters such as fractional anisotropy (FA) and apparent diffusion coefficient along with generation of fiber tractography maps. We investigated DTI using single shot echo planar imaging in 20 diffusion directions on 3T MRI in nine patients diagnosed with intradural spinal tumors and found significant reduWction in FA value within the lesion compared to FA value at normal cord. Tractography maps generated by DTI were useful in differentiating intramedullary from extramedullary location of tumor. Tractography also provided useful information regarding tract infiltration or displacement in cases of intramedullary neoplasms. Thus, DTI proved helpful in classification, characterization, and treatment planning of intradural spinal tumors.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"45 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116325030","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
Antenatal diagnosis of Sirenomelia, the Mermaid syndrome with bilateral renal agenesis 双侧肾发育不全的双侧肾缺血症、美人鱼综合征的产前诊断
Case Reports in Clinical Radiology Pub Date : 2023-03-13 DOI: 10.25259/crcr_25_2022
Ankita Rani, Moinuddin Sultan
{"title":"Antenatal diagnosis of Sirenomelia, the Mermaid syndrome with bilateral renal agenesis","authors":"Ankita Rani, Moinuddin Sultan","doi":"10.25259/crcr_25_2022","DOIUrl":"https://doi.org/10.25259/crcr_25_2022","url":null,"abstract":"A 26-year-old non-diabetic primigravida with 4 months of amenorrhea was appointed for a routine second-trimester anomaly scan. On inspection, the gravid abdominal girth of the lady did not correlate with her gestational age. Ultrasonographic examination showed a single live intrauterine gestation with anhydramnios. There was an absence of bilateral kidneys and urinary bladder with lying down adrenal sign suggestive of bilateral renal agenesis. The fetus also revealed caudal dysgenesis in the form of fusion of both lower limbs, seen as a single leg with 1 upturned foot and fused toes. There were no identifiable external genitalia and anus. The parents went ahead with medical termination of pregnancy after being informed about the condition and its incompatibility with life.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"61 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131151598","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
Meckel’s diverticulitis with abscess presentation in an acute abdomen 急性腹部伴有脓肿的梅克尔憩室炎
Case Reports in Clinical Radiology Pub Date : 2023-03-13 DOI: 10.25259/crcr_15_2023
Pavankumar Suraparaju Varaprasadvarma, A. Pawar, V. Kaginalkar
{"title":"Meckel’s diverticulitis with abscess presentation in an acute abdomen","authors":"Pavankumar Suraparaju Varaprasadvarma, A. Pawar, V. Kaginalkar","doi":"10.25259/crcr_15_2023","DOIUrl":"https://doi.org/10.25259/crcr_15_2023","url":null,"abstract":"The vitellointestinal/omphalomesenteric duct is embryonic structure connecting primary yolk sac to the embryonic midgut which obliterates by 10th week of gestation. It may persist or incompletely obliterate to form anomalies like Meckel’s diverticulum that is most common and is usually asymptomatic. Symptoms develop when Meckel’s diverticulum involves complications such as hemorrhage, inflammation, and perforation, or when it causes intussusception or bowel obstruction. The modalities useful in diagnosing it are ultrasonography (USG) and computed tomography (CT), USG being more easily available, and radiation free is the first modality useful to suspect these anomalies. It can mimic close differentials such as appendicitis and urachal anomalies. In this case report, a 12-year-old male child presented with recurrent periumbilical pain who was screened on USG was suspected Meckel’s diverticulitis with abscess; the same was confirmed on contrast CT scan and managed surgically. This case shows the importance of USG and radiologist’s suspicion of Vitellointestinal duct anomalies in diagnosing and its associated complications.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116193603","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 report of pediatric anterior urethral diverticulum arising at the bulbar urethra 小儿前尿道憩室发生于尿道球部1例
Case Reports in Clinical Radiology Pub Date : 2023-03-13 DOI: 10.25259/crcr_14_2022
P. R. Gadhari, S. Ghatge
{"title":"Case report of pediatric anterior urethral diverticulum arising at the bulbar urethra","authors":"P. R. Gadhari, S. Ghatge","doi":"10.25259/crcr_14_2022","DOIUrl":"https://doi.org/10.25259/crcr_14_2022","url":null,"abstract":"Congenital anterior urethral diverticulum at the bulbar urethra is a rare entity. Accumulation of urine within the diverticulum causes obstruction to the free flow of urinary stream and resultant symptoms such as difficulty in micturition, dribbling of urine, and urinary tract infection. Correct recognition of this condition is important to initiate early surgical treatment. Micturating cystourethrogram and ultrasonography are imaging modalities of choice for identification and surgical planning of this entity.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122195112","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 report: Renal coloboma syndrome 肾结肠瘤综合征1例报道
Case Reports in Clinical Radiology Pub Date : 2023-03-13 DOI: 10.25259/crcr_48_2022
M. Makada, C. Dhandhalya, Mihir Joshi, R. Patel
{"title":"A rare case report: Renal coloboma syndrome","authors":"M. Makada, C. Dhandhalya, Mihir Joshi, R. Patel","doi":"10.25259/crcr_48_2022","DOIUrl":"https://doi.org/10.25259/crcr_48_2022","url":null,"abstract":"Renal coloboma syndrome (RCS), also called papillorenal syndrome, is a rare syndrome characterized by renal abnormalities and optic nerve dysplasia. We present a case of a neonate with renal and eye abnormalities. Along with the known diagnosis of multicystic dysplastic kidney, the neonate was diagnosed with coloboma of the right eye, making a probable diagnosis of RCS. Retinal detachment and decreased visual acuity are implications of the ocular malformations. Hypertension, proteinuria, and renal insufficiency, which frequently lead to end-stage kidney disease, are serious consequences of renal dysplasia.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"46 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128696322","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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