Podocytic infolding in Schimke immuno-osseous dysplasia with novel SMARCAL1 mutations: a case report
Autor: | Qing-Nan He, Xiao-Chuan Wu, Xiqiang Dang, Shiqiu Xiong, Lanjun Shuai, Xiaoyan Li |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Male
0301 basic medicine Spondyloepiphyseal dysplasia Pathology medicine.medical_specialty Arteriosclerosis Primary Immunodeficiency Diseases Nephrotic syndrome Case Report Gene mutation Osteochondrodysplasias lcsh:RC870-923 Schimke immuno-osseous dysplasia 03 medical and health sciences Focal segmental glomerulosclerosis Glomerulopathy Internal medicine medicine Humans 030102 biochemistry & molecular biology Podocytes business.industry Glomerular basement membrane DNA Helicases medicine.disease lcsh:Diseases of the genitourinary system. Urology Podocytic infolding glomerulopathy Microscopy Electron 030104 developmental biology medicine.anatomical_structure Nephrology Dysplasia Child Preschool Pulmonary Embolism business |
Zdroj: | BMC Nephrology, Vol 21, Iss 1, Pp 1-5 (2020) BMC Nephrology |
ISSN: | 1471-2369 |
DOI: | 10.1186/s12882-020-01809-6 |
Popis: | Background Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive disorder characterized by spondyloepiphyseal dysplasia, progressive renal insufficiency and defective cellular immunity. Podocytic infolding glomerulopathy (PIG) is a newly proposed disease entity characterized by microspheres or microtubular structures associated with podocytes infolding into the glomerular basement membrane (GBM) on electron microscopy (EM). Case presentation A 4-year-old boy was admitted to our ward due to proteinuria and edema lasting 1 month. He had a short trunk and demonstrated subtle dysmorphology, with a triangular shape, a broad nasal bridge and a bulbous nasal tip. The laboratory findings were as follows: lymphocytes, 0.5 × 109/L; urine protein, 3.67 g/d; albumin, 9.8 g/L; and cholesterol, 11.72 mmol/L. Skeletal X rays showed small iliac wings, small ossification centers of the capital femoral epiphyses, shallow dysplastic acetabular fossae and mildly flattened vertebrae. The specimen for light microscopy (LM) suggested focal segmental glomerulosclerosis (FSGS). EM revealed a focal thickness of the GBM with some cytoplasmic processes of podocyte infolding into the GBM. Gene sequencing showed novel compound heterozygous mutations in the SMARCAL1 gene (c.2141 + 5G > A; c.2528 + 1G > A) that were inherited from his parents. Finally, we established the diagnosis of SIOD and treated him with diuretics and angiotensin-converting enzyme inhibitors (ACEIs). Conclusion The pathogenic mechanism of PIG has not been clarified. Further studies are required to understand whether gene mutations, especially those related to podocytes, contribute to the pathogenesis of podocytic infolding. |
Databáze: | OpenAIRE |
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