Results 41 to 50 of about 10,688 (221)

Metabolic myopathy presenting with polyarteritis nodosa: a case report

Journal of Medical Case Reports, 2011
Introduction To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa.
Elbalkhi Amro, Abdullah Mishal, Vishwanath Sahana, Ambrus Julian L   +3 more
doaj   +1 more source

Beyond Raynaud's: Atypical Peripheral Vascular Manifestations in a Case of CREST Syndrome

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Peripheral vascular disease (PVD) is a rare but severe symptom of CREST syndrome, which itself is a limited cutaneous sclerosis. Even though Raynaud's phenomenon is the gold standard of CREST, the development of critical limb ischemia and self‐amputation is rare.
Sakshi Kumari, Fathimathul Henna, Umama Alam, Fazia Khattak, Kamil Ahmad Kamil   +4 more
wiley   +1 more source

Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa

Einstein (São Paulo)
Arthritis has been reported as an acute pattern, generally evanescent with oligoarthritis, mostly affecting knees and ankles in childhood systemic polyarteritis nodosa.
Glaucia Vanessa Novak, Koken Hayashi, Kohei Sampa, Yosuke Okumura, Gabriela Ribeiro Viola Ferreira, Clovis Artur Silva   +5 more
doaj   +1 more source

Consensus Statement on Precision Anatomy and Treatment Strategies for Median Arcuate Ligament Syndrome: AOB Consensus Meeting

Asian Journal of Endoscopic Surgery, Volume 19, Issue 1, January/December 2026.
ABSTRACT Background With the increasing use of minimally invasive surgery, understanding of the precise anatomy involved in median arcuate ligament syndrome (MALS) has advanced. However, surgical strategies and treatment principles for MALS remain unclear.
Hidenori Haruta, Masaharu Higashida, Katsuyuki Hoshina, Toshio Takayama, Tomotaka Ueno, Saya Chiba, Noboru Ideno, Naoki Ikenaga, Shunji Endo, Yasunaru Sakuma, Toshiya Abe, Kenoki Ouchida, Masafumi Nakamura, Yuko Kitagawa, Akiko Umezawa   +14 more
wiley   +1 more source

Giant Coronary Artery Aneurysm due to Polyarteritis Nodosa in an Eight-Year-Old Child [PDF]

, 2021
Maza Olga Cecilia, Gallon Carlos Alberto, Echeverria Rafael Vicente, Morales Cristina Isabel, John Jairo Araujo   +4 more
openalex   +1 more source

Pyoderma Gangrenosum as the First Manifestation of Inflammatory Bowel Disease: A Case Report

Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.
Approximately 50% of patients with inflammatory bowel disease (IBD) exhibit extraintestinal manifestations, among which skin and mucosal lesions are common. However, pyoderma gangrenosum occurs in only 1%‐2% of IBD patients. We report the case of a 23‐year‐old male patient who was admitted to the hospital with pyoderma gangrenosum that was unresponsive
Nam Hoai Nguyen, Tan Thi Tran, Trang Thu Khuc, Yen Thi Lo, Ha Thi-Ngoc Doan, Hieu Van Nguyen, Long Cong Nguyen, Marcel Cc Machado   +7 more
wiley   +1 more source

Cutaneous polyarteritis nodosa: A case report with a brief review of literature

Medical Journal of Dr. D.Y. Patil University, 2013
Polyarteritis nodosa (PAN) is a rare vasculitis with multisystem involvement. The definition, diagnostic criteria and validity of cutaneous polyarteritis nodosa (c-PAN) as a variant of classic PAN limited to skin have continued to remain disputed.
Yugal K Sharma, Kedarnath Dash, Neha Goyal, Neha C Virmani   +3 more
doaj   +1 more source

Cutaneous polyarteritis nodosa

British Journal of Dermatology, 2002
Classic polyarteritis nodosa (PAN) is a segmentary leucocytoclastic vasculitis that affects small- and medium-sized arteries. In 1931, Lindberg (Acta Med Scand 1931; 76: 183-225) described the existence of a cutaneous variant of PAN, without visceral involvement and with a more favourable prognosis. We present four patients diagnosed with cutaneous PAN
España, A. (Agustín), Idoate, M.A. (Miguel Ángel), Bauza, A. (Ana)   +2 more
openaire   +3 more sources

A Rare Case of Giant Cell Arteritis Affecting Two Giants: Pulmonary and Root of Aorta Aneurysm

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Aneurysms of pulmonary arteries and aorta are rare, typically caused by infections, congenital heart defects, vascular abnormalities, or medical interventions. This report presents an unusual case of a 72‐year‐old man with a history of smoking, hypertension, and emphysema, who was found to have a large pulmonary artery aneurysm (63.5 mm) and ...
Gajendra Acharya, Hafiza Baloch, Pradeep Masuta, Rohit Pandit, Robert Kimelheim, Prabal Tiwari   +5 more
wiley   +1 more source

Spontaneous kidney rupture in a patient with polyarteritis nodosa

Journal of Research in Medical Sciences, 2006
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-sized arteries. It involves the renal arterioles in approximately 80% of cases, but spontaneous retroperitoneal hemorrhage is a rare complication of ...
Ahmad Mohammadi, Mohammad Reza Gharaati, Mohammad Reza Ebadzadeh   +2 more
doaj