eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | vasculitis |
| Symptom | C0034150|purpura |
| Sentences | 18 |
| PubMedID- 26019477 | We concluded that henoch-schonlein purpura, a kind of leukocytoclastic vasculitis, might have contributed to the development of the bruising. |
| PubMedID- 24574837 | In anca(+) patients, renal involvement, neuropathy, alveolar hemorrhage, and vasculitis with purpura are predominant, while in anca(-) patients, cardiac and pulmonary involvement are predominant . |
| PubMedID- 19597730 | Renal cell carcinoma presenting as henoch-schonlein purpura with leukocytoclastic vasculitis, hematuria, proteinuria and abdominal pain. |
| PubMedID- 26509054 | Lesions other than purpura and supposedly due to vasculitis such as isolated urticarial or macular rash of vasculitic origin should be confirmed (by histology and/or the presence of cryoglobulins) at least once in patient history. |
| PubMedID- 21855727 | Palpable purpura is indicative of leukocytoclastic vasculitis, and is an early, critical sign in rickettsial diseases, including rocky mountain spotted fever, which must be diagnosed and treated early. |
| PubMedID- 25268749 | Multinomial analyses were performed by distinguishing three groups of pss: (i) purpura associated with cryoglobulinaemic vasculitis (cv), (ii) purpura associated with hypergammaglobulinaemic vasculitis (hgv), and (iii) pss patients without purpura (pss controls). |
| PubMedID- 23151856 | Henoch-schonlein purpura (hsp) is one of the most common vasculitis syndromes affecting children. |
| PubMedID- 22982638 | Symptoms related to ads, such as autoimmune thyroiditis, type 1 diabetes mellitus, coeliac disease, juvenile idiopathic arthritis, dermatomyositis, autoimmune haemolytic anaemia, leukocytoclastic vasculitis, henoch-schonlein purpura, hypoparathyroidism, alopecia areata, addison's disease, vitiligo and systemic lupus erythematosus were detected in these patients, who have been followed with diagnosis of pid including common variable immunodeficiency, selective and partial iga deficiency, wiskott-aldrich syndrome, ataxia telangiectasia, hyperimmunoglobulin e syndrome, chronic mucocutaneous candidiasis, griscelli syndrome, and partial c4 deficiency.immunodeficiency and autoimmune phenomenon may concomitantly present in an individual, although they seem to be incompatible ends in the spectrum of the clinical immune response. |
| PubMedID- 21729687 | We report the case of an uncommon presentation of an iga lambda multiple myeloma in a 58 year-old woman preceded by vascular purpura with cutaneous leukocytoclastic vasculitis (lv) and intense deposit of iga and kappa light chains in the dermal vessels. |
| PubMedID- 23773652 | Flare of essential mixed cryoglobulinemic vasculitis with hemorrhagic bullous purpura after rituximab infusion. |
| PubMedID- 20549478 | Besides the typical lupus forms, nonspecific skin lesions are also observed such as dermal mucinosis, acneiform skin lesions, different variants of livedo, necrotizing vasculitis with ulcers, purpura, urticaria vasculitis, neutrophilic dermatosis, hyperpigmentation, hair and nail changes as well as overlap syndromes with erythema multiforme, scleroderma, sjogren syndrome, raynaud phenomenon, lichen planus, bullous pemphigoid und psoriasis. |
| PubMedID- 25688001 | Iga vasculitis (henoch-shonlein purpura) in adults: diagnostic and therapeutic aspects. |
| PubMedID- 21722330 | The classic triad of hsp is purpura (due to leucocytoclastic vasculitis of small skin vessels), arthritis and abdominal pain (due to gastrointenstinal vasculitis). |
| PubMedID- 24007933 | Then henoch-schonlein purpura with abdominal vasculitis was suspected, and later confirmed by histopathology. |
| PubMedID- 24265897 | This report describes a rare presentation of henoch-schonlein purpura with coronary vasculitis which leads to myocardial infarction at the age of 53. |
| PubMedID- 21188196 | In these patients, typical symptoms are fatigue and palpable purpura, which histologically consists of a leukocytoclastic vasculitis (with complexes of anti-hcv and hcv in injured tissue); see figure 1. |
| PubMedID- 25294333 | This disease is a leukocytoclastic vasculitis sharing features with schonlein-henoch purpura, but with a more benign self-limiting course with minimal risk of organ involvement. |
| PubMedID- 21870104 | Skin vasculitis, with palpable purpura clinically and leukocytoclastic vasculitis on pathological examination, is common. |
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