Results 51 to 60 of about 2,648 (158)

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

Hydroxyurea‐Associated Wunderlich Syndrome in Triple‐Negative Myelofibrosis: A Case Report and Literature Review

Case Reports in Hematology, Volume 2026, Issue 1, 2026.
Background Wunderlich syndrome (WS) is a spontaneous, nontraumatic intrarenal or perirenal hemorrhage most commonly related to renal neoplasms, vascular disorders, infection, cyst rupture, or anticoagulation. Clinical severity ranges from self‐limited bleeding to hemorrhagic shock.
Veysel Erol, Zeki Güzel, İbrahim Ethem Akgün, Gökhan Ecer, Rounak Dubey   +4 more
wiley   +1 more source

Inflammatory bowel disease and immune-mediated inflammatory diseases: looking at the less frequent associations

Therapeutic Advances in Gastroenterology, 2022
Patients with inflammatory bowel disease (IBD) often have other immune-mediated inflammatory diseases (IMIDs), and the prevalence of any IMID is higher in IBD patients than in the general population.
Cristina Bezzio, Cristina Della Corte, Marta Vernero, Imma Di Luna, Gianpiero Manes, Simone Saibeni   +5 more
doaj   +1 more source

Bilateral Renal Artery Thrombosis With Distal Abdominal Aortic Dissection as the First Presentation of Takayasu Arteritis

Case Reports in Nephrology, Volume 2026, Issue 1, 2026.
Background Takayasu arteritis (TAK) is a chronic granulomatous large‐vessel vasculitis that predominantly affects the aorta and its major branches, leading to stenosis, occlusion, or aneurysmal changes. Renal artery disease is common, but acute bilateral renal artery thrombosis causing renal dysfunction is rare.
Mihiran Thanigasalan, Mehatheepan Rasanayagam, Mathu Selvarajah, Poorani Gurumallesh Prabu   +3 more
wiley   +1 more source

Poliarterite nodosa cutânea na infância com gangrena digital e possível associação com o estreptococo beta-hemolítico do grupo a: relato de caso e revisão de literatura Cutaneous polyarteritis nodosa in children presenting with digital gangrene and possible association with group a beta hemolytic streptococcus infection

Revista Brasileira de Reumatologia, 2008
A poliarterite nodosa cutânea (PAN cutânea) é uma forma particular de vasculite envolvendo artérias de pequeno e médio calibres. A doença pode ser diferenciada da poliarterite nodosa sistêmica pela sua limitação à pele e ausência de envolvimento visceral.
Karina Silva Marins, Ronaldo Baptista, Vladimir Nentzinsky, Mário Newton Leitão de Azevedo, Blanca Elena Rios Gomes Bica   +4 more
doaj   +1 more source

Rare Presentation of Sinonasal Synovial Sarcoma With Frontal Sinus and Limited Intracranial Extension Associated With Probable Paraneoplastic Vasculitis: A Case Report

Case Reports in Surgery, Volume 2026, Issue 1, 2026.
Synovial sarcoma is a high‐grade soft‐tissue sarcoma that commonly affects adolescents and young adults. Involvement of the head and neck region is rare, and tumors arising from the sinonasal tract are particularly uncommon and diagnostically challenging.
Afnan W. M. Jobran, Ibrahim Alzatari, Yazan Abugharbieh, Mohammed Abdulrazzak, Hasan Arafat, Neetu Rawal   +5 more
wiley   +1 more source

Misdiagnosed for 14 Years: Adenosine Deaminase 2 (ADA2) Deficiency in a Teen Mimicking Polyarteritis Nodosa

Clinical Case Reports
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disorder caused by loss of function mutations in the ADA2 gene (previously the CECR1 gene) on chromosome 22q11.
Mohammadkian Zarafshani, Masoume Avateffazeli, Seyed Masoud Moeini Taba, Reihaneh Faghihi, Sara Beikmohamadi Hezaveh, Vahid Ziaee, Fatemeh Tahghighi, Maryam Loghman   +7 more
doaj   +1 more source

Classic polyarteritis nodosa presenting initially as a case of cutaneous polyarteritis nodosa: A case report

Asian Journal of Medical Sciences
Classic polyarteritis nodosa (PAN) is an uncommon form of aggressive systemic vasculitis involving small-to-medium sized arteries usually of renal vasculature and other visceral organs but characteristically sparing the lung vasculature. Cutaneous PAN (c-
Sabina Adhikari
doaj   +1 more source

Essential Thrombocythemia's Role in the Complex Landscape of Vasculitis: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Peripheral gangrenes have been sporadically documented as the initial presentation of essential thrombocythemia (ET), as exemplified in the preceding case reports. Nevertheless, the prevalence of vasculitis‐induced skin problems as the primary indication of ET has not been extensively examined.
Mohammad Reza Jafari Nakhjavani, Seyedeh‐Tarlan Mirzohreh, Sousan Kolahi, Mehrzad Hajialilo, Mehdi Jafarpour, Arezou Ghassembaglou, Mir Ali Sattary Oskouie, Tala Pourlak, Sepideh Tahsini Tekantapeh   +8 more
wiley   +1 more source

Never say never

Journal of Hospital Medicine, Volume 21, Issue 2, Page 200-204, February 2026.
Gurpreet Dhaliwal, Jagmeet Dhingra, Tom Fraser, Leal Herlitz, James Pile   +4 more
wiley   +1 more source