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Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
Clinical features of children with pulmonary microscopic polyangiitis: report of 9 cases
Haiyan Wang1, Liangzhong Sun2, Weiping Tan1
1Department of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, Peoples' Republic of China.
Abstract:
Kidneys and lungs are the most common organs involved in microscopic polyangiitis (MPA). A retrospective analysis of pediatric MPA patients with pulmonary lesions over the past 10 years was performed to investigate clinical features of MPA in children with pulmonary lesions. There were 9 patients enrolled in our study, including 2 boys and 7 girls, with a median age of 6.6 years at the time of disease onset and a median disease course of 2 months. All of the patients exhibited tachypnea, and 7 exhibited cough and hemoptysis. The most common presentation on pulmonary imaging was ground glass or patchy shadows, which were observed in 6 cases. Seven patients manifested with hematuria and proteinuria, with renal histopathology of fibrinoid necrosis/exudation of the glomerular capillaries. All of the patients presented with normocytic normochromic anemia. Of the 9 patients, 7 were positive for perinuclear antineutrophil cytoplasmic antibody (p-ANCA) and/or myeloperoxidase (MPO), and 2 were positive for p-ANCA/MPO and cytoplasmic ANCA/proteinase 3. Eight patients had normal complement 3 (C3) levels, and one had an elevated C3 level. Five of the 9 patients were positive for antinuclear antibody ANA, and 4 were positive for double strand DNA (ds-DNA) antibody (3 were positive for both). The 7 patients who exhibited renal involvement received steroid plus cyclophosphamide (CTX) treatment. Of these patients, 4 achieved various degrees of remission, 2 were at the beginning of induction therapy, and one was lost to follow-up. Two patients with isolated pulmonary involvement received steroid plus leflunomide treatment and achieved complete remission. Diffuse alveolar hemorrhage was the most frequent presentation of lung involvement in children with MPA, and tachypnea, cough, hemoptysis and anemia were the common clinical symptoms. The majority of these patients exhibited hematuria, proteinuria and renal insufficiency. The efficacy of steroid plus CTX or leflunomide was evident in these patients.
Insights
Microscopic polyangiitis (MPA) in children often involves the lungs and kidneys. Early treatment with steroids and cyclophosphamide or leflunomide showed promising remission rates in pediatric MPA patients with pulmonary lesions.
Area of Science:
- Pediatric Rheumatology
- Pulmonary Medicine
- Nephrology
Background:
- Microscopic polyangiitis (MPA) is a rare autoimmune vasculitis affecting small blood vessels.
- Kidneys and lungs are frequently involved organs in MPA, particularly in pediatric cases.
- Understanding the clinical manifestations and treatment outcomes in children with pulmonary involvement is crucial.
Observation:
- This study analyzed 9 pediatric MPA patients with pulmonary lesions over 10 years.
- Common symptoms included tachypnea, cough, hemoptysis, and anemia.
- Pulmonary imaging often showed ground glass or patchy shadows, indicative of diffuse alveolar hemorrhage.
Findings:
- Seven patients presented with renal involvement (hematuria, proteinuria) and characteristic glomerular fibrinoid necrosis.
- Most patients tested positive for perinuclear antineutrophil cytoplasmic antibody (p-ANCA) and/or myeloperoxidase (MPO).
- Treatment with steroids plus cyclophosphamide (CTX) or leflunomide demonstrated efficacy, with several patients achieving remission.
Implications:
- Diffuse alveolar hemorrhage is a key lung manifestation in pediatric MPA.
- Prompt diagnosis and treatment are essential for favorable outcomes in children with MPA.
- The study highlights the effectiveness of current therapeutic strategies in managing pediatric MPA with lung and kidney involvement.
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