دورية أكاديمية

Henoch-Schönlein Purpura Associated with Pulmonary Adenocarcinoma ; Púrpura de Henoch-Schönlein Associada a Adenocarcinoma do Pulmão

التفاصيل البيبلوغرافية
العنوان: Henoch-Schönlein Purpura Associated with Pulmonary Adenocarcinoma ; Púrpura de Henoch-Schönlein Associada a Adenocarcinoma do Pulmão
المؤلفون: Azevedo, A, Fernandes, V, Navarro, D, Ferreira, AC, Sousa, J, Viana, H, Carvalho, F, Nolasco, F
بيانات النشر: Sociedade Portuguesa de Nefrologia
سنة النشر: 2015
المجموعة: Repositório do Centro Hospitalar de Lisboa Central EPE
مصطلحات موضوعية: HCC NEF, Purpura, Schönlein-Henoch, Lung Neoplasms, Renal Insufficiency, Vasculitis
الوصف: Introduction: The Henoch-Schönlein purpura (HSP) is an immunoglobulin A (IgA)-mediated smallvessel systemic vasculitis, rare in adults. The association with solid tumours has been described, especially with lung cancer. Case Report: We present the case of a 60-year-old Caucasian male, diagnosed with lung adenocarcinoma that underwent surgical resection without (neo)adjuvant theraphy. Two months latter he was admitted for abdominal pain, purpuric rash on his lower extremities and acute kidney injury, with serum creatinine (Scr) of 2 mg/dl. Urinalysis revealed haematuria and 24h proteinuria (P24h) of 1.5 g. The serum protein electrophoresis, complement components C3 and C4, circulating immune complexes, cryoglobulins, ANCA, ANA, anti-dsDNA and the remaining immunologic study as screening for viral infections (HCV, HBV and HIV) were negative. Renal ultrasound was normal and kidney biopsy revealed mild mesangial proliferation; 2 cellular glomerular crescents and 1 fibrinoid necrosis lesion; large amounts of red blood cell casts; lymphocytic infiltration in the intertubular interstitial capillaries; moderate arteriolar hyalinosis. Immunofluorescence demonstrated mesangial and parietal deposits of IgA. The diagnosis of HSP was assumed, and the patient started prednisolone 1 mg/kg/day. Ten months after diagnosis the patient’s baseline Scr is 1.4 mg/dl with P24h of 0.18g, without haematuria. Conclusion: Although this is a rare association and the exact mechanism behind the disease is yet unknown, physicians should be aware of it. The early recognition and treatment may prevent renal disease progression.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: Port J Nephrol Hypert 2015; 29 (3): 248-252; http://hdl.handle.net/10400.17/2414Test
الإتاحة: http://hdl.handle.net/10400.17/2414Test
حقوق: openAccess
رقم الانضمام: edsbas.EBCB6506
قاعدة البيانات: BASE