1.Predominant tubulointerstitial lupus nephritis in a case.
Jian-ping HUANG ; Xin LI ; Jing-jing ZHANG ; Yuan-hua ZONG ; Jing-cheng LIU ; Ji-yun YANG
Chinese Journal of Pediatrics 2004;42(3):221-221
Child
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Humans
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Lupus Nephritis
;
complications
;
Male
;
Nephritis, Interstitial
;
etiology
;
Prognosis
3.Treatment of Primary Sjögren's Syndrome Complicated Nephritis of Henoch-Schonlein Purpura: a Case Report of One Case.
Chang-chang LIANG ; Qiao-qiao LIU ; Tian YU
Chinese Journal of Integrated Traditional and Western Medicine 2015;35(12):1526-1527
Humans
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Nephritis
;
etiology
;
therapy
;
Prognosis
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Purpura, Schoenlein-Henoch
;
complications
;
therapy
;
Sjogren's Syndrome
;
etiology
;
therapy
4.A case of shunt nephritis.
Ho Seok LEE ; Sung Ho CHA ; Byoung Soo CHO ; Moon Ho YANG
Journal of Korean Medical Science 1995;10(1):62-65
Nephritis associated with a chronically infected ventriculoatrial shunt is known as shunt nephritis. A 6-year-old girl with prior history of a ventriculoatrial shunt presented complaining of fever and gross hematuria. Serum complement levels were decreased and a coagulase-negative S. epidermidis was cultured from her blood. The renal biopsy specimen showed features of membranoproliferative glomerulonephritis type I. Hydrocephalus was so severe that shunt removal was impossible. With antibiotic therapy, clinical symptoms and laboratory findings include complement levels were normalized although microscopic hematuria persisted. To our knowledge, this is the first case of shunt nephritis in Korea. In addition to the case report, a brief review of shunt nephritis has been added.
Case Report
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Child
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Female
;
Human
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Nephritis/*etiology
;
Ventriculoperitoneal Shunt/*adverse effects
7.Intensive reading of evidence-based guidelines on diagnosis and treatment of childhood common renal diseases (II).
Song-ming HUANG ; Qiu LI ; Yan-fang GUO
Chinese Journal of Pediatrics 2009;47(12):914-916
Child
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Evidence-Based Medicine
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Humans
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Nephritis
;
diagnosis
;
etiology
;
therapy
;
Practice Guidelines as Topic
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Purpura
;
complications
;
diagnosis
;
therapy
8.A Case of Systemic Lupus Erythematosus Presenting as Malignant Hypertension with Hypertensive Retinopathy.
Jung Yoon CHOE ; Sung Hoon PARK ; Ji Young KIM ; Hyun Young JUNG ; Seong Kyu KIM
The Korean Journal of Internal Medicine 2010;25(3):341-344
The variability of cardiovascular abnormalities is one of the characteristics of systemic lupus erythematosus (SLE). Among the cardiovascular manifestations, hypertension is reported in 14% to 58.1% of patients in diverse ethnic populations, and remains a clinically important issue due to its close relationship with early mortality in patients with SLE. The development of hypertension in patients with SLE has been associated with advanced lupus-related renal disease and the medications used for the treatment of lupus. Malignant hypertension is a serious complication of hypertension; it rarely occurs in patients with SLE. However, it can occur in patients with other complicated medical conditions such as the antiphospholipid antibody syndrome (APS) or cardiac tamponade. Here, we report the case of a patient with SLE and malignant hypertension with hypertensive retinopathy that initially presented without clinical evidence of APS or hypertensive nephropathy.
Adult
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Female
;
Humans
;
Hypertension, Malignant/*diagnosis/*etiology
;
Lupus Erythematosus, Systemic/*complications/*diagnosis
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Lupus Nephritis/complications/diagnosis
;
Retinal Diseases/*diagnosis/*etiology
10.Fechtner syndrome, a nonmuscle myosin heavy chain 9 gene mutation related disease: a case report and literature review.
Rui HU ; Ji-hong HAO ; Hong-le YANG ; Yun ZHU ; Shun-yi LI ; Jie ZHAO ; Feng-ru LIN ; Zhi-yun NIU
Chinese Journal of Hematology 2011;32(2):103-106
OBJECTIVETo improve the recognition of Fechtner syndrome.
METHODSThe clinical and laboratory data and family survey of a patient with Fechtner's syndrom was reported.
RESULTS AND CONCLUSIONGiant platelets, thrombocytopenia and characteristic granulocyte inclusion bodies (Döhle-like bodies) were found in both peripheral blood and bone marrow smears of the patient. Clinically the patient had renal damage, nervous deafness, and vitreous lesions. There was a family genetic tendency on family survey the diagnosis of Fechtner syndrome is established.
Hearing Loss, Sensorineural ; etiology ; genetics ; Humans ; Male ; Middle Aged ; Molecular Motor Proteins ; genetics ; Mutation ; Myosin Heavy Chains ; genetics ; Nephritis, Hereditary ; etiology ; genetics ; Thrombocytopenia ; etiology ; genetics