Hydrophilic polymer microembolism with cutaneous involvement observed incidentally in a patient undergoing endovascular procedures: a case report

2016 ◽  
Vol 43 (7) ◽  
pp. 632-634 ◽  
Author(s):  
Keisuke Goto ◽  
Toshihiro Takai ◽  
Kazuyuki Nishimura ◽  
Yoshimi Oshitani
Keyword(s):  
Case Report ◽  
Endovascular Procedures ◽  
Hydrophilic Polymer ◽  
Cutaneous Involvement

scholarly journals Retrieval of a migrated N-butyl-2 cyanoacrylate cast using a snare-kit system during dural AVF embolization: A case report

2018 ◽  
Vol 24 (5) ◽  
pp. 571-573
Author(s):  
Ramy Ahmed ◽  
Satomi Ide ◽  
Hiro Kiyosue ◽  
Shuichi Tanoue ◽  
Shunro Matsumoto ◽  
...  
Keyword(s):  
Case Report ◽  
Arteriovenous Fistula ◽  
Dural Arteriovenous Fistula ◽  
Endovascular Procedures ◽  
Sigmoid Sinus ◽  
Embolic Material ◽  
Coagulation Profile ◽  
Liquid Embolic

N-butyl-2 cyanoacrylate (NBCA) is a liquid embolic material that is widely used in various endovascular procedures because of its permanent and rapid vascular occluding effect regardless of the coagulation profile of the patient. However, NBCA migration to unintended vessels may result in serious complications. This report describes the retrieval of a migrated NBCA cast from the transverse-sigmoid sinus during dural arteriovenous fistula embolization using a transvenous snaring technique.

scholarly journals Photodistributed sarcoidosis: a case report and approach to management

2018 ◽  
Vol 6 ◽  
pp. 2050313X1879687
Author(s):  
Cristina Olteanu ◽  
Brandon Worley ◽  
Iris Teo ◽  
Jillian Macdonald
Keyword(s):  
Case Report ◽  
Ionizing Radiation ◽  
Bone Pain ◽  
Prior Exposure ◽  
Systemic Involvement ◽  
Pruritic Rash ◽  
Cutaneous Involvement ◽  
Multiple Organs ◽  
History Of ◽  
Idiopathic Disease

Sarcoidosis is an idiopathic disease, characterized by non-caseating granulomas in multiple organs/tissues. Cutaneous involvement occurs in approximately one-quarter of patients with a wide variety of presenting morphologies. This case report describes a case of photodistributed sarcoidosis, a rare cutaneous variant, with systemic involvement. A 42-year-old man presented with a history of a pruritic, rash with photoexacerbated annular plaques along with arthralgias and bone pain. Compared to previous reports of photodistributed sarcoidosis, our case presented with annular plaques rather than papules, and there was no prior exposure to ionizing radiation. He was treated successfully with prednisone and hydroxychloroquine. It is important to include sarcoidosis in the differential of photodistributed dermatoses.

scholarly journals Cerebral Proliferative Angiopathy: Case Report

2018 ◽  
Vol 37 (02) ◽  
pp. 131-133 ◽  
Author(s):  
Luana Gatto ◽  
Rodrigo Brisson ◽  
Zeferino Demartini ◽  
Gelson Koppe ◽  
Carlos Rocha
Keyword(s):  
Case Report ◽  
Endovascular Procedures ◽  
Brain Parenchyma ◽  
Neurological Deficits ◽  
Motor Deficit ◽  
Brain Arteriovenous Malformation ◽  
Cerebral Vascular Disease ◽  
Functional Brain ◽  
History Of ◽  
Over Time

AbstractProliferative angiopathy (PA) is a rare cerebral vascular disease in which anomalous vessels continually recruit additional feeder arteries, amid a functional brain parenchyma. We report the case of a young woman with progressive history of headache, motor deficit, seizures and drowsiness. She received a misdiagnosis of brain arteriovenous malformation (AVM) and evolved with dysarthria and cognitive decline after an unsuccessful embolization performed at another institution. We opted for conservative treatment with periodic control by imaging tests. Proliferative angiopathy differs in natural history, prognosis, histopathology and treatment of the usual AVMs. Endovascular procedures aggravate the neurological deficits, which are usually progressive and tend to worsen over time.

Hydrophilic polymer microemboli in a patient with a chronic cutaneous ulcer: a case report

2014 ◽  
Vol 41 (12) ◽  
pp. 955-958 ◽  
Author(s):  
Sepehr Hamidi ◽  
Ryan Stevens ◽  
Brittney DeClerck ◽  
Gene H. Kim
Keyword(s):  
Case Report ◽  
Hydrophilic Polymer ◽  
Cutaneous Ulcer

Crystal-Deficient Alveolar Soft-Part Sarcoma With Cutaneous Involvement: A Case Report

2009 ◽  
Vol PAP ◽  
Author(s):  
Denisa Kacerovska ◽  
Michal Michal ◽  
Jana Nemcova ◽  
Tomas Vanecek ◽  
Boris Kreuzberg ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Part ◽  
Alveolar Soft Part Sarcoma ◽  
Cutaneous Involvement

scholarly journals Endovascular treatment of vein of Galen aneurysmal malformation using rapid ventricular pacing: A case report

2016 ◽  
Vol 23 (1) ◽  
pp. 97-101 ◽  
Author(s):  
Birgitta Ramgren ◽  
Olof Rask ◽  
Jan Gelberg ◽  
Petru Liuba ◽  
Per Undrén ◽  
...  
Keyword(s):  
Case Report ◽  
Endovascular Treatment ◽  
Endovascular Procedures ◽  
High Flow ◽  
Vein Of Galen ◽  
Ventricular Pacing ◽  
Rapid Ventricular Pacing

The treatment of choice of vein of Galen aneurysmal malformation (VGAM) involves endovascular procedures that can be difficult to perform in high-flow fistulas. We describe the use of rapid ventricular pacing (RVP), a well-known cardiologic technique, to safely treat a high-flow fistula in an infant with VGAM.

Childhood sarcoidosis: A case report

2021 ◽  
Author(s):  
Phuong Anh Le Thi
Keyword(s):  
Case Report ◽  
Skin Biopsy ◽  
Clinical Features ◽  
Early Onset ◽  
Unknown Etiology ◽  
Cutaneous Involvement ◽  
Multisystem Involvement ◽  
First Choice ◽  
Granulomatous Lesions ◽  
Granulomatous Disorder

Childhood sarcoidosis is a rare multisystemic granulomatous disorder of unknown etiology. The diagnosis is often delayed due to lacking of recognition of clinical features. We report a 23 month-old boy who presented with multiple pinkish papules and painless cystic swellings in his ankles and wrists. A skin biopsy showed multiple sarcoidal granulomatous lesions. He was treated with steroids and had a good response. Childhood sarcoidosis is characterized by arthritis, uveitis, and cutaneous involvement. Glucocorticoids remain the first choice therapy for children with multisystem involvement. The prognosis of early-onset childhood sarcoidosis varies in different studies due to the rarity of the disease.

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