Results 41 to 50 of about 11,626 (181)

Safely Treating a Pulmonary Embolism in a Patient With Hereditary Hemorrhagic Telangiectasia: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant bleeding disorder. The incidence of venous thromboembolisms among HHT patients is significantly greater than the general population. However, providing therapeutic anticoagulation in patients with an increased propensity for bleeding creates a clinical dilemma.
Christina Carfagnini, Manasa Kandula
wiley   +1 more source

Anticardiolipin antibodies in patients with Behcet's disease

Biomolecules & Biomedicine, 2011
The aims of this study are to determine anticardiolipin antibodies in patients with Sy Behcet and to determine correlation between the levels of anticardiolipin antibodies in serum in patients with clinic systemic and ocular manifestations.
Maja Zivkovic, Marko Zlatanovic, Gordana Zlatanovic, Jasmina Djordjevic-Jocic, Sonja Cekic   +4 more
doaj   +1 more source

Catastrophic Antiphospholipid Syndrome in a Young Female Complicated by Systemic Lupus Erythematosus and Left Atrial Myxoma: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed, Mohammad Nazrul Hossain, Abdullah Salman, Sabrina Yesmin, S. M. G. Saklayen   +4 more
wiley   +1 more source

Reverse Diagnostic Thinking for Aortic Coarctation Using the Renal Artery Bilateral Parvus et Tardus as a Clue: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT In young patients with hypertension or stroke, the presence of bilateral parvus et tardus waveforms in the renal arteries should prompt reverse tracing to rule out aortic coarctation. This simple ultrasound clue enables early, non‐invasive screening and prevents missed diagnoses.
Yan‐li Chen, Jin‐hua Wang
wiley   +1 more source

Diagnosis and Management of Catastrophic Antiphospholipid Syndrome and the Potential Impact of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria

Antibodies
Catastrophic antiphospholipid syndrome (CAPS) is a rare and life-threatening condition characterized by the persistence of antiphospholipid antibodies and occurrence of multiple vascular occlusive events. CAPS currently remains a diagnostic challenge and
Lucas Jacobs, Nader Wauters, Yahya Lablad, Johann Morelle, Maxime Taghavi   +4 more
doaj   +1 more source

High Prevalence of aCL-IgA and aβ2GPI-IgA in Drug-Free Schizophrenia Patients: Evidence of a Potential Autoimmune Link

Antibodies
Background/Objectives: Schizophrenia (SZ) is a complex psychiatric disorder with increasing evidence pointing to an autoimmune component, including the presence of antiphospholipid antibodies (aPLs).
Samar Samoud, Imen Zamali, Fatma Korbi, Ahlem Mtiraoui, Ahlem Ben Hmid, Neila Hannachi, Yousr Galai, Hechmi Louzir, Yousri El Kissi   +8 more
doaj   +1 more source

Úlceras de pernas e anticorpos anticardiolipinas Leg ulcers and anticardiolipin antibodies

Anais Brasileiros de Dermatologia, 2011
Fenômenos pró-trombóticos são descritos em úlceras de perna de diferentes etiologias. Neste trabalho, procurou-se verificar a prevalência de anticorpos anticardiolipina nestes pacientes.
Thelma Larocca Skare
doaj   +1 more source

Long‐Term Dermoscopic Evolution of Reticular Erythematous Mucinosis: Case Report

JEADV Clinical Practice, Volume 5, Issue 2, Page 637-639, June 2026.
ABSTRACT Reticular erythematous mucinosis is a rare dermatosis with a challenging diagnosis. To date, its dermoscopic features have not been well characterised in the literature. Only a limited number of case reports have described dermoscopic findings that may be indicative of the disorder, including the presence of dotted and linear vessels, as well ...
Grażyna Kamińska‐Winciorek, Karolina Zarańska, Anastazja Szlauer‐Stefańska, Jacek Pająk, Sebastian Giebel   +4 more
wiley   +1 more source

Clinical Utility of Stillbirth Investigations in Australia: A Cohort Study

Australian and New Zealand Journal of Obstetrics and Gynaecology, Volume 66, Issue 3, June 2026.
ABSTRACT Background Stillbirths impact over two million parents globally every year. Despite current knowledge, technology, and investigations, many stillbirths remain unexplained and are not fully investigated. An important step forward in addressing this gap is determining which investigations produce the highest utility in identifying the cause of ...
Tania Marsden, Mu Cheng, T. Yee Khong, Jane E. Dahlstrom, David Ellwood, Ali Moghimi, Stacey Prystupa, Cecilia Obrien, Fathima S. Cassim, Skye Martin, Michael Coory, Frances M. Boyle, Heidi Shukralla, Alison L. Kent, Ashwati Krishnan Varikara, Patricia Hannaford, Joanne Frost, Joanna Perry‐Keene, Gretchen Pomare, Yin Ping Wong, Geok Chin Tan, Vicki Flenady, Jessica Sexton   +22 more
wiley   +1 more source

Anticardiolipin syndrome: antiphospholipid syndrome [PDF]

Clinical Medicine, 2001
La detection d'anticorps antiphospholipides est a l'origine du syndrome des antiphospholipides caracterise par des pathologies vasculaires et des fausse-couches chez la femme ...
openaire   +2 more sources