Results 81 to 90 of about 16,344 (265)
Churg-Strauss Syndrome with Necrosis of Toe Tips [PDF]
, 2011 Churg-Strauss syndrome (CSS) is a granulomatous necrotizing vasculitis of unknown etiology associated with bronchial asthma. Despite affecting small to medium-sized vessels, necrosis of the digits due to vasculitis is extremely rare.
Hasegawa, Kenjiro +9 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Adult‐onset Still's disease (AOSD) is a rare, multisystem autoinflammatory disorder characterized by a classic triad of fever, evanescent rash, and arthritis with diagnostic challenges. We present a case of a previously healthy 22‐year‐old Nepalese female presented with a 1.5‐month history of progressive bilateral lower limb edema and a 13‐day
Sushil Silwal +3 more
wiley +1 more source
A GIANT ANEURYSM OF PROPER HEPATIC ARTERY IN A CRYOGLOBULINEMIC PATIENT ON HEMODIALYSIS: A CASE REPORT. [PDF]
, 2014 Introductrion. Hepatic artery aneurysms (HAAs) are unusual vascular lesions often associated with many different pathological conditions. Most of reported cases are described in association with connective tissue diseases, such as polyarteritis nodosa ...
Cerasola, G. +7 more
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Catastrophic secondary antiphospholipid syndrome with peripheral nervous system involvement: a case report. [PDF]
, 2004 A 34-year-old woman was admitted to our emergency room with a high fever, abdominal pain, dyspnea and confusion. High fever and abdominal pain had first occured after a cystocele operation 5 months earlier.
Erten, Nilgun +5 more
core +1 more source
Coexistence of Takayasu Arteritis and Intestinal Tuberculosis in a Young Bangladeshi Woman
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Takayasu arteritis (TAK) is a rare, chronic, granulomatous large‐vessel vasculitis predominantly affecting young women. Although its etiology remains uncertain, tuberculosis (TB) has long been implicated as a potential trigger. We report a 28‐year‐old Bangladeshi woman with TAK coexisting with transverse colon TB, a rare but clinically ...
Suchismita Debnath +5 more
wiley +1 more source
Autoantibodies in systemic vasculitis [PDF]
, 2015 Systemic vas culitis is a heterogeneous group of disorders characterized by inflammation and necrosis in the vessel wall. the diagnosis of a systemic vasculitis is challenging, because patients usually present a broad spectrum of manifestations that vary
Souza, Alexandre Wagner Silva de
core +3 more sources
Dysautonomia in a cutaneous polyarteritis nodosa patient: evidence of systemic evolving? [PDF]
Beyond RheumatologyObjective: We report a case of a patient with a cutaneous polyarteritis nodosa who developed dysautonomia and review this association's literature. Case report: A 75-year-old male patient was admitted with a recent history of recurrent ulcers on his ...
J. de Carvalho +2 more
doaj +1 more source
Journal of Internal Medicine, Volume 299, Issue 2, Page 196-215, February 2026.Abstract Cryoglobulinemia (CG) is defined by the presence of serum immunoglobulins that precipitate below 37°C and redissolve upon rewarming. It is classified into three types based on immunoglobulin composition. Type I, a rare form, involves monoclonal IgM or IgG and is linked to lymphoproliferative disorders.
Anna Linda Zignego +7 more
wiley +1 more source
Síndrome de Churg-Strauss - Vasculite Cutânea como Forma de Apresentação Clínica [PDF]
, 2009 A síndrome de Churg-Strauss (SCS) ou angeíte granulomatosa alérgica é uma doença rara caracterizada pela presença de asma, eosinofilia e vasculite dos pequenos e, por vezes, dos médios vasos.
João, A +4 more
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New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]
, 1984 The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter +3 more
core +1 more source