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Case Reports in Radiology

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https://www.readbyqxmd.com/read/30073109/abernethy-malformation-type-ii-and-concurrent-nodular-hyperplasia-in-a-rare-female-case
#1
Zhen Kang, Xiangde Min, Liang Wang
Background: Abernethy malformation is a rare splanchnic vascular abnormality characterizing extrahepatic abnormal shunts that is classified into types I and II. Abernethy malformation type I has a female predilection and is associated with a variety of concurrent hepatic benign or malignant tumours while type II with concurrent tumours is very rare in females. Case Report: We report a rare female case of Abernethy malformation type II with concurrent occupying lesion in the right liver, which was successfully transplanted; the occupying lesion was pathologically proven to be nodular hyperplasia...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/30057844/metastatic-renal-cell-carcinoma-presenting-as-prolonged-pyrexia-and-stauffer-s-syndrome-can-a-routine-ultrasound-scan-fail-to-detect-a-renal-cell-carcinoma
#2
C L Fonseka, A G T A Kariyawasam, S A G L Singhapura, C M de Silva, T E Kanakkahewa, I G T M Senarathna, C K Bodinayake
Background: Prolonged pyrexia and weight loss are recognised paraneoplastic manifestations of renal cell carcinoma (RCC). Stauffer's syndrome is a rarely described paraneoplastic manifestation, which is described early in the course of RCC. We report a patient who presented with unresolving fever with multiple pulmonary opacities with biochemical evidence of hepatic choleastasis and was later diagnosed to have metastatic RCC with Stauffer's syndrome. Case Presentation: We report a 54-year-old female who was investigated for a poorly resolving fever and recent weight loss for two months...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/30026995/rhinogenic-optic-neuritis-caused-by-sphenoid-mucocele-with-sinusitis
#3
Sasitorn Siritho, Weerachai Tantinikorn, Paithoon Wichiwaniwate, Krit Pongpirul
A 59-year-old male who presented with a nonspecific headache at the vertex, resembling retrobulbar optic neuritis, was treated as such but did not show any improvement. Although optic nerve compression from sphenoid mucocele was finally discovered, the delayed diagnosis and improper treatment led to a permanent visual loss. Optic neuritis could be caused by a common problem, "mucocele/sinusitis," but might be easily overlooked in general practice. Rhinogenic optic neuropathy should, therefore, be considered in every case of optic neuritis whenever atypical presentation occurs or is unresponsive to high-dose steroid treatment...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/30009075/mandibular-osteitis-leading-to-the-diagnosis-of-sapho-syndrome
#4
Tomohiro Kikuchi, Hiroyuki Fujii, Akifumi Fujita, Tomoko Sugiyama, Hideharu Sugimoto
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a disorder characterized by pustular skin lesions and osteoarticular lesions. Mandibular involvement of SAPHO syndrome is clinically rare, and it is difficult to reach a diagnosis of SAPHO syndrome from only mandibular manifestations. This report describes the case of a 26-year-old woman who presented with mandibular osteitis. Orthopantomogram and computed tomography showed sclerotic change of the right body of the mandible with periosteal reaction without odontogenic infection, which suggested the possibility of SAPHO syndrome...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29992075/endovascular-embolization-of-spontaneous-iliopsoas-hematoma-first-experience-with-squidperi
#5
Pierluca Torcia, Silvia Squarza, Umberto G Rossi, Paolo Rigamonti, Lorenzo Carlo Pescatori, Giovanni Damiani, Maurizio Cariati
A 79-year-old man, suffering from atrial fibrillation and on anticoagulation therapy, was admitted at the emergency department of our institution because of a worsening respiratory insufficiency. After a diagnostic work-up, he was found to suffer from pneumonia, and antibiotic therapy was settled. He was kept under observation for his pulmonary conditions but, within a week, he developed a spontaneous iliopsoas hematoma, due to a sudden dysregulation of anticoagulation therapy subsequent to new in-hospital treatments...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29984032/sarcoid-of-the-upper-humerus-found-incidentally-on-mr-images-obtained-for-work-up-of-rotator-cuff-tear-where-compromised-tissue-quality-was-a-concern-for-surgical-success
#6
Tanner R Henrie, John G Skedros
Sarcoidosis is an idiopathic systemic inflammatory disorder characterized histologically by noncaseating granulomas. The pathogenesis likely includes genetic, immunologic, and environmental factors. The lungs, skin, and eyes are most commonly affected. Although bone involvement is possible, sarcoidosis of the humerus is rare, with few cases reported. Furthermore, we are unaware of any reports of sarcoidosis of the upper humerus with a coexisting rotator cuff tear. We report the case of a 50-year-old female with sarcoidosis of the humerus and a coexisting tear of the supraspinatus tendon...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29971177/parotid-oncocytoma-as-a-manifestation-of-birt-hogg-dub%C3%A3-syndrome
#7
Kazuki Yoshida, Masao Miyagawa, Teruhito Kido, Kana Ide, Yoshifumi Sano, Yoshifumi Sugawara, Hiroyuki Takahata, Nobuya Monden, Mitsuko Furuya, Teruhito Mochizuki
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disease characterized by skin fibrofolliculomas, pulmonary cysts, spontaneous pneumothoraces, and renal cancers. Oncocytomas are benign epithelial tumors that are also rare. Recently, there have been a few case reports of BHD with a parotid oncocytoma that appears to have a BHD phenotype. Here we document the eighth known case and describe the magnetic resonance imaging features of the parotid oncocytoma, which mimicked Warthin's tumor. Radiologists should be aware of the association between these rare disorders...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29888021/sacral-myeloid-sarcoma-manifesting-as-radiculopathy-in-a-pediatric-patient-an-unusual-form-of-myeloid-leukemia-relapse
#8
Joana Ruivo Rodrigues, Manuel João Brito, Rui Pedro Faria Pais, Sílvia Carvalho
Myeloid sarcoma (MS), granulocytic sarcoma or chloroma, is defined as a localized extramedullary mass of blasts of granulocytic lineage with or without maturation, occurring outside the bone marrow. MS can be diagnosed concurrently with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). The authors report a case of sacral MS occurring as a relapse of myeloid leukemia in a 5-year-old girl who was taken to the emergency department with radiculopathy symptoms.
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29862112/massive-hematemesis-from-a-splenic-artery-pseudoaneurysm-presenting-two-years-after-penetrating-trauma
#9
Geraldine Abbey-Mensah, Michael M Herskowitz, James Walsh, Robert F Leonardo
Splenic artery pseudoaneurysms (PSA) are rare entities and far less common than true aneurysms of the splenic artery. The most common etiology is pancreatitis, recurrent either in the setting of chronic pancreatitis or as an episode of acute pancreatitis. Less common causes include trauma, peptic ulcer disease, or iatrogenic causes. Almost all of the trauma-related case reports have been due to blunt trauma. We believe this to be the first reported case of a splenic artery PSA presenting with massive hematemesis at a significant time frame after penetrating trauma...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29862111/a-thymic-hyperplasia-case-without-suppressing-on-chemical-shift-magnetic-resonance-imaging
#10
Tuan Phung, Thach Nguyen, Dung Tran, Nga Phan, Hung Nguyen
A 22-year-old woman with myasthenia gravis (MG) presented with ptosis and mild muscle weakness symptoms for one year. Computed tomography (CT) presented a diffuse bilobulate enlargement gland with a high density of soft tissue. Magnetic resonance imaging (MRI) showed the gland with no suppression on the opposed-phase chemical shift. After the thymic tumor diagnosis, she underwent thoracoscopic surgery for tumor resection. The postoperative histopathological finding was thymic lymphoid hyperplasia. This case suggests chemical shift MRI is not enough in distinguishing, and supplementary examination is essential to avoid unnecessary thymic biopsy and surgery...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29862110/case-report-of-hydatid-cyst-in-the-pulmonary-artery-uncommon-presentation-ct-and-mri-findings
#11
Arwa Almutairi, Sulaiman Al Rajhi
Background: Hydatid cysts can be found in any organ. In adults, the liver and lungs are the most common locations; hydatid cysts in the pulmonary artery are rare. Clinical Case: We present the case of an 86-year-old female with a history of hepatic hydatid cyst since 2012, who presented with complaints of chronic productive cough, yellowish-green sputum, and dyspnea. CT and MRI showed multiseptate hydatid cysts in the right pulmonary artery.
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29854536/primary-pulmonary-anaplastic-large-cell-lymphoma-a-rare-malignancy-and-rare-cause-of-the-luftsichel-sign
#12
Elizabeth Von Ende, Travis Kauffman, Philip A Munoz, Santiago Martinez-Jiménez
Primary pulmonary lymphomas are rare with primary pulmonary non-Hodgkin lymphoma accounting for only 0.3% of primary lung neoplasms. Of these, the large majority are made up of marginal zone B-cell lymphoma and diffuse large B-cell lymphoma. We present a case of a very rare primary pulmonary anaplastic large cell lymphoma presenting as the luftsichel sign on chest radiograph. Pertinent imaging and pathology findings are discussed.
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29854535/septic-embolic-stroke-followed-by-hemorrhage-and-brain-abscess-in-a-patient-with-systemic-infections-a-case-report-and-literature-review
#13
Jama A Mohamud, Jingtao Wu, Ye Jing, Yu Wang
We report a case of 50-year-old man with a severe acute ischemic stroke followed by intracerebral hemorrhage and brain abscess due to systemic infection. His initial intracranial radiographic findings were normal but three days later MRI scan of the brain revealed well-defined rounded cystic lesion on the T2-weighted and T1-weighted images in the right basal ganglia; the lesion presented an area of diffusion restriction on DWI; lately the lesion was confirmed to be an early stage of cerebral abscess. A week later the patient was noted to have worsening neurological status and left extremity weakness, and emergency brain CT scan revealed massive intracerebral hemorrhage in the right occipital lobe; he underwent intracranial hematoma evacuation surgery...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29854534/perfusion-imaging-in-autoimmune-encephalitis
#14
Deepak Vallabhaneni, Muhammad Atif Naveed, Rajiv Mangla, Awss Zidan, Rashi I Mehta
Encephalitis is characterized by inflammation of brain tissue and has various infectious and noninfectious causes. CSF analysis and MRI usually reveal inflammatory changes although sometimes brain imaging may be normal. Autoimmune encephalitis is caused by antibodies against neuronal synaptic receptors, surface proteins, or intracellular proteins. In this case report, we present a 65-year-old female who presented with a fall and altered mental status. Workup for infectious etiologies was negative and MRI of the brain displayed focal restricted diffusion with corresponding T2-FLAIR hyperintensity involving gray matter structures, making the diagnosis unclear...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29850356/an-unusual-pediatric-case-of-allen-key-penetrating-trauma-in-maxillofacial-region
#15
Feride Fatma Görgülü, Orhan Görgülü, Ayşe Selcan Koç, Fatma Yasemin Öksüzler
Paranasal sinus (PNS) foreign bodies are not common. They are usually due to penetrating trauma and iatrogenic events. On imaging, radiopaque foreign bodies can easily be detected by X-ray views of PNS. CT scan may be necessary to evaluate the exact location of foreign body in some cases. Foreign body in the PNS should be removed as early as possible. Approach and technique of its removal depend upon its size, shape, and location. Nasal endoscopic examination can be helpful for these cases. We present a pediatric girl case of penetrating FB injury inserted into the maxillary sinus towards nasopharynx in a suddenly braking car...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29850355/rosai-dorfman-disease-rare-pulmonary-involvement-mimicking-pulmonary-langerhans-cell-histiocytosis-and-review-of-the-literature
#16
Rashid Al Umairi, Danielle Blunt, Wedad Hana, Matthew Cheung, Anastasia Oikonomou
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder. We report a patient with RDD who presented with multiple skin lesions, pulmonary involvement, and CT manifestations mimicking Langerhans cell histiocytosis, which improved after initiation of corticosteroid treatment.
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29850354/intravascular-large-b-cell-lymphoma-presenting-with-diffuse-gallbladder-wall-thickening-a-case-report-and-literature-review
#17
Sayf Al-Katib, Robert Colvin, Farnoosh Sokhandon
Intravascular large B-cell lymphoma is a rare subtype of extranodal diffuse B-cell lymphoma characterized by proliferation of neoplastic cells within the lumen of small and medium sized vessels. Clinical and imaging findings are nebulous as the intravascular subtype of lymphoma can involve a multitude of organs. Involvement of the gallbladder is extremely uncommon, and imaging findings can be easily confused for more prevalent pathologies. We report a case of intravascular large B-cell lymphoma in an 83-year-old male and review clinical presentation and imaging findings on CT, ultrasound, hepatobiliary iminodiacetic acid (HIDA) scan, and MRI...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29785317/a-rare-case-of-penile-metastases-as-a-harbinger-of-primary-pulmonary-adenosquamous-carcinoma
#18
Partha Hota, Tejas N Patel, Xiaofeng Zhao, Carrie Schneider, Omar Agosto
Although lung cancer has a high propensity for distant metastatic disease, penile metastases from primary lung neoplasms are considered particularly rare. A 71-year-old male presented to our hospital with a rapidly enlarging hard palpable penile mass. MR imaging demonstrated two penile masses centered in the left and right corpus cavernosa. Subsequent CT imaging revealed a spiculated pulmonary mass in the right upper lobe with PET/CT, MRI, and surgical exploration, demonstrating evidence of metastases to the left adrenal gland, right subscapularis muscle, brain, and small bowel...
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29721344/urethral-duplication-with-a-cystic-phallic-urethra-associated-with-a-uterus-didelphys-partial-agenesis-of-the-tibia-and-an-equinovarus-foot
#19
Edwige Kafando, Boniface Moifo, Landry Mbouche, Derek Ndangoh, Evelyn Mah, Faustin Mouafo Tambo
Urethral duplication is a rare congenital malformation, especially in females. It may be associated with complex urogenital malformations, but the association with a cystic phallic urethra and a uterus didelphys is exceptional. We report a case of a newborn with urethral duplication, with the accessory urethra exteriorized by a large cyst, associated with a uterus didelphys and bone malformations. We discuss the clinical, radiographic, and therapeutic aspects as well as a literature review.
2018: Case Reports in Radiology
https://www.readbyqxmd.com/read/29682386/extraosseous-intradural-chondrosarcoma-of-the-cervical-spine-a-case-report-with-brief-review-of-literature
#20
Elizabeth Presutto, Sejal Patel, Joseph Fullmer, Sajeev Ezhapilli
Mesenchymal chondrosarcoma (MCS) is a malignant cancer of the cartilage that accounts for less than 1% of all chondrosarcomas and typically occurs within the bone. One-third of all mesenchymal chondrosarcomas are extraosseous soft tissue sarcomas, rendering this as an uncommon entity. We report a rare case of an extraosseous chondrosarcoma with the cervical spinal canal in a 21-year-old male. The purpose of this case report is to discuss the imaging characteristics of this pathology proven diagnosis.
2018: Case Reports in Radiology
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