Spontaneous cervical epidural hemorrhage, anterior cord syndrome, and familial vascular malformations: Case report

Microsurgery ◽  
1980 ◽  
Vol 1 (6) ◽  
pp. 457-460
Author(s):  
Dominic Foo ◽  
Young C. Chang ◽  
Alain B. Rossier
2020 ◽  
Vol 36 (12) ◽  
pp. 3147-3152
Author(s):  
Helen J. Zhang ◽  
Nicole Silva ◽  
Elena Solli ◽  
Amanda C. Ayala ◽  
Luke Tomycz ◽  
...  

2021 ◽  
Vol 14 (9) ◽  
pp. e241649
Author(s):  
Raj Patel ◽  
Edward James Durant ◽  
Robert Freed

This case report describes a 20-year-old woman presenting to the emergency department (ED) with unilateral leg swelling. After multiple visits to the ED and workups with rheumatology, dermatology, interventional radiology and genetics, she was finally diagnosed with Parkes-Weber syndrome. The purpose of this case report is to illustrate the common and uncommon presentations, mimickers and work-up of Parkes-Weber syndrome as well as provide a brief overview of vascular malformations in general.


2006 ◽  
Vol 28 (8) ◽  
pp. 720-723 ◽  
Author(s):  
Leanne S. Dahlgren ◽  
Sidney B. Effer ◽  
Barbara C. McGillivray ◽  
Denise J. Pugash

2019 ◽  
Vol 10 (02) ◽  
pp. 339-341 ◽  
Author(s):  
Santosh P. V. Rai ◽  
Shrijeet Chakraborti ◽  
Parvathi Chandran ◽  
Muralidhar V. Pai

ABSTRACTCavernomas are vascular malformations which are collections of endothelium-lined sinusoids without intervening cerebral parenchyma. Hypothalamic location of cavernoma is extremely rare. We present a case of a 34-year-old male who presented with complaints of recent memory loss and vomiting. On magnetic resonance imaging with gradient sequences and contrast, a diagnosis of hypothalamic cavernoma was suggested. Excision of lesion was performed by a right parasagittal pericoronal craniotomy via transcallosal approach. Intraoperative findings and histopathology examination corroborated the diagnosis. The uniqueness of this case report is in the susceptibility-weighted sequence which led to the radiological diagnosis.


2013 ◽  
Vol 5 (2) ◽  
pp. 91-93
Author(s):  
Hitesh Verma

ABSTRACT Cavernous hemangiomas are relatively rare vascular malformations especially in an adult. The childhood hemangioma generally regresses spontaneously. We present the case report of a 52-year-old male patient, who had a hemangioma from the childhood and it had grown to such a large size so as to cause extreme cosmetic deformity for the patient. The long standing duration of almost 45 years and the extremely large size of the hemangioma make it a very rare case. How to cite this article Gupta N, Verma H. Large and Long Standing Cavernous Hemangioma of Cheek. Int J Otorhinolaryngol Clin 2013;5(2):91-93.


2018 ◽  
Vol 05 (03) ◽  
pp. 190-192
Author(s):  
Rajashree Uday Gandhe ◽  
Chinmaya Pradeep Bhave ◽  
Avinash Sahebarav Kakde ◽  
Kalyani Anand Sathe

AbstractAirway management of patients with craniofacial vascular malformations poses many challenges. Establishment of a secure airway is a prerequisite for safe anesthetic management of these patients. We report a case of a 45-year-old man presenting with a facial vascular malformation involving the tongue, parapharynx, and extending into the neck, resulting in airway compromise scheduled for endovascular embolization.


HPB Surgery ◽  
2010 ◽  
Vol 2010 ◽  
pp. 1-4 ◽  
Author(s):  
Guillermo Sangster ◽  
Daniel Do ◽  
Carlos Previgliano ◽  
Benjamin Li ◽  
Delecia LaFrance ◽  
...  

Paragangliomas are extra-adrenal tumors of the autonomic nervous system and may be found within the skull base, neck, chest, and abdomen. When presenting within the abdominal cavity, they may arise as a primary retroperitoneal neoplasm and can mimic vascular malformations or other conditions related to specific retroperitoneal organs such as the pancreas, kidneys, or adrenals. Retroperitoneal paragangliomas are mostly benign with good prognosis; however, they can present with abdominal pain, palpable mass, or hypertensive episodes. Patients should be initially evaluated with catecholamine levels, followed by computed tomography or magnetic resonance imaging to locate the primary lesion. Surgical excision remains the mainstay of treatment, although advanced disease and proximity to vital organs can make excision difficult or impossible. This case report describes a patient who initially underwent work up for a suspected pancreatic head mass which was discovered to be a retroperitoneal paraganglioma by frozen section.


1994 ◽  
Vol 34 (12) ◽  
pp. 825-828 ◽  
Author(s):  
Takuya AKAI ◽  
Yoshiki MINO ◽  
Michiharu NISHIJIMA ◽  
Naoya KUWAYAMA ◽  
Akira TAKAKU

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