Platelet-derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder |
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Authors: | Ogawa Jiro Kanegane Hirokazu Tsuneyama Koichi Kanezaki Rika Futatani Takeshi Nomura Keiko Ishizawa Shin Sasahara Masakiyo Ito Etsuro Miyawaki Toshio |
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Affiliation: | Department of Pediatrics;, First Department of Pathology Graduate School of Medicine, University of Toyama, Toyama;;Department of Pediatrics, Hirosaki University of School of Medicine, Hirosaki;;Second Department of Pathology, Graduate School of Medicine, University of Toyama, Toyama, Japan |
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Abstract: | Transient myeloproliferative disorder (TMD) is experienced by approximately 10% of neonates with Down syndrome (DS). Most TMD is asymptomatic and the patients undergo spontaneous remission within a few months. However, some cases are fatal because of systemic organ dysfunctions including hepatic fibrosis. Some cytokines such as platelet-derived growth factor (PDGF) may be involved in the development of hepatic fibrosis in TMD. The report describes a fatal case of TMD accompanying DS. The patient presented with pulmonary hypertension and hepatic failure. An autopsy disclosed severe fibrosis in the lung, liver, kidney and pancreas. Immunohistochemical analysis revealed high expression of PDGF receptor beta in the severe fibrotic areas of the fibrotic tissues. A real-time polymerase chain reaction (PCR) analysis demonstrated the expression of PDGFalpha and PDGFbeta in the peripheral blood samples of the patient. The finding indicates that the PDGF pathway may play an important role in the fibrosis of several organs in patients with TMD. |
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Keywords: | Down syndrome fibrosis platelet-derived growth factor transforming growth factor-β1 transient myeloproliferative disorder |
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