Results 51 to 60 of about 10,688 (221)
Spontaneous Retroperitoneal Hematoma: A Rare Presentation of Polyarteritis Nodosa
Spontaneous retroperitoneal hematoma is a rare clinical entity that is most commonly caused by renal tumors and vascular disease. In this article, we present a case of spontaneous retroperitoneal hemorrhage caused by polyarteritis nodosa in a patient who
Asad Ullah MD +4 more
doaj +1 more source
ABSTRACT Takayasu arteritis (TAK) is a rare large‐vessel vasculitis affecting the aorta and its major branches. Although autoimmune mechanisms are central, prior mycobacterial infections have been hypothesized to contribute to the disease onset. A 55‐year‐old South Asian woman with a history of vitiligo and treated multibacillary leprosy presented with
Ujjawal Bhattarai +7 more
wiley +1 more source
Polyarteritis nodosa with uterine involvement [PDF]
Polyarteritis nodosa (PAN) is characterized by multisystem necrotizing vasculitis, primarily affecting small-to-medium-sized muscular arteries, and it is typically found in middle-aged men.
Chihiro Hirai +6 more
doaj +1 more source
The correlation of the clinical and postmortem findings shows that there is no close relationship between the syndrome of polyarteritis nodosa and the allergic states, that pain is the most common symptom, that congestive heart failure is the common cause of death.
GEORGE C. GRIFFITH, I. LUTFI VURAL
openaire +1 more source
ABSTRACT Objective Autoimmunity can be part of the pathogenesis of polycystic ovary syndrome (PCOS), but prospective studies on autoimmune disease in population based cohorts are lacking. This study aimed to investigate incidence rates of autoimmune disease in Danish women with PCOS before and after PCOS diagnosis compared to controls.
Dorte Glintborg +4 more
wiley +1 more source
Childhood polyarteritis nodosa: A rare presentation
Polyarteritis nodosa (PAN) is a rare systemic vasculitis characterized by necrotizing arteritis of small to medium-sized arteries. It manifests as skin ulceration, hypertension, abdominal pain, digital gangrene, subcutaneous nodules etc.
Sandeep Lahiry
doaj +1 more source
The Impact of Complement Factor H‐Related Protein Gene Deletions on Kidney Transplantation
In this study, we found that rs7542235 allele G tags a deletion of the CFHR1 gene. We also found that rs6677604 allele A tags a deletion of the whole CFHR3–1 locus. The plasma proteomics studies show that both variants are associated with an altered expression of FH/FHR proteins thus revealing a novel level of intricate regulation of the complement ...
Salla Markkinen +6 more
wiley +1 more source
Central illustration summarizing the comprehensive case management of Takayasu arteritis in a 40‐year‐old female. The figure integrates key aspects: vascular pathology (left subclavian occlusion, right subclavian narrowing, 4.0 cm infrarenal aneurysm), clinical presentation (right arm pain, neck stiffness), inflammatory markers (CRP 18.4 mg/L, ESR 45 ...
Sakib Abrar +5 more
wiley +1 more source
Dysautonomia in a cutaneous polyarteritis nodosa patient: evidence of systemic evolving? [PDF]
Objective: 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

