RESUMO
A 33-year-old male patient with abdominal mass for a year was referred to our institute. CT scan with intravenous contrast was performed, which showed a cystic lesion at the infraumbilical region, beneath the anterior abdominal wall with the presence of solid enhancing mass apposed to the anterior wall of the cyst. We suggested a diagnosis of urachal cyst with possibility of malignancy. On surgical exploration, the cystic mass was found superior to and separate from the urinary bladder dome. Histopathology revealed transitional cell carcinoma in a urachal cyst.
Assuntos
Carcinoma de Células de Transição/diagnóstico por imagem , Tomografia Computadorizada por Raios X/métodos , Cisto do Úraco/diagnóstico por imagem , Neoplasias da Bexiga Urinária/diagnóstico por imagem , Adulto , Carcinoma de Células de Transição/patologia , Carcinoma de Células de Transição/cirurgia , Meios de Contraste , Diagnóstico Diferencial , Humanos , Masculino , Cisto do Úraco/patologia , Cisto do Úraco/cirurgia , Neoplasias da Bexiga Urinária/patologia , Neoplasias da Bexiga Urinária/cirurgiaAssuntos
Aorta Torácica/anormalidades , Aorta Torácica/diagnóstico por imagem , Doenças da Aorta/diagnóstico por imagem , Anormalidades Cardiovasculares/diagnóstico por imagem , Divertículo/diagnóstico por imagem , Artéria Subclávia/anormalidades , Artéria Subclávia/diagnóstico por imagem , Tomografia Computadorizada por Raios X/métodos , Feminino , Humanos , MasculinoRESUMO
Persistent left superior vena cava is a rare finding seen only in 0.3%-0.5% population. It is generally asymptomatic and is often discovered after central venous catheterization done for various indications. We present a case where we demonstrate persistent left superior vena cava/left cardinal vein remnant discovered during left-sided cuffed catheter insertion for hemodialysis in a 65-year-old chronic kidney disease patient. Findings were confirmed with computed tomography venogram. This anomaly poses iatrogenic risks to the patient if not detected early. A catheter along the left mediastinal border can be dangerously close to descending aorta and could also be indicative of its placement in the internal thoracic vein or, pericardiophrenic vein. It can also perforate the persistent/remnant vessel and enter the pleura, pericardium, or mediastinum. This case emphasizes the importance of familiarity with this entity and its role in determining the appropriate venous access for patient therapy when faced with this clinical situation.
Assuntos
Cateterismo Venoso Central/instrumentação , Cateteres Venosos Centrais , Achados Incidentais , Veia Cava Superior Esquerda Persistente/complicações , Diálise Renal , Insuficiência Renal Crônica/terapia , Idoso , Cateterismo Venoso Central/efeitos adversos , Cateteres de Demora , Angiografia por Tomografia Computadorizada , Humanos , Masculino , Veia Cava Superior Esquerda Persistente/diagnóstico por imagem , Flebografia , Insuficiência Renal Crônica/complicações , Insuficiência Renal Crônica/diagnóstico , Resultado do TratamentoRESUMO
We report the clinical details and imaging findings for a case of nondecussating retinal-fugal fiber syndrome or isolated achiasma in a 4-year-old female child. Findings included the isolated absence of optic chiasm with unremarkable rest of the optic pathway and midline structures in a child presenting clinically with see-saw nystagmus. Clinically congenital see-saw nystagmus, "mirror reversal" of visual field representation and interocular ipsilateral asymmetry on monocular visual evoked potential point toward achiasma and warrant further evaluation with magnetic resonance imaging (MRI). Isolated achiasma is a rare condition that may remain undiagnosed unless MRI is done.
Assuntos
Anormalidades do Olho/diagnóstico por imagem , Imageamento por Ressonância Magnética , Fibras Nervosas/patologia , Nistagmo Congênito/diagnóstico por imagem , Quiasma Óptico/anormalidades , Células Ganglionares da Retina/patologia , Vias Visuais/anormalidades , Pré-Escolar , Feminino , HumanosRESUMO
We report the clinical details and imaging findings for a case of vesicovaginal reflux presenting as gross urocolpos in a 15-year-old female. Findings included a large fluid-filled vagina on full-bladder scan in the absence of any anatomical abnormality, which disappeared completely after micturition. It is important for radiologists to be aware of this entity as it is rarely encountered and leads to very confusing findings, which could result in an erroneous diagnosis.
Assuntos
Hidrocolpos/diagnóstico por imagem , Hidrocolpos/etiologia , Doenças da Bexiga Urinária/complicações , Doenças da Bexiga Urinária/diagnóstico por imagem , Adolescente , Diagnóstico Diferencial , Feminino , Humanos , Hidrocolpos/urina , Tomografia Computadorizada por Raios X , Doenças da Bexiga Urinária/urina , Micção , Vagina/diagnóstico por imagemRESUMO
We report the clinical details and imaging findings of a case of perforated Littre's hernia presenting as lower abdominal wall cellulitis in a 50-year-old male. Findings included herniation of an oral contrast opacified blind-ending pouch arising from the anti-mesenteric border of the distal ileum into the right inguinal canal, with extravasation of oral contrast. There were adjacent inflammatory changes with subcutaneous emphysema extending up to the right anterior chest wall. Meckel's diverticulum is rarely diagnosed preoperatively on imaging. We highlight the importance of computed tomography in imaging Meckel's diverticulum.