Platelet-derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder

Jiro Ogawa, Hirokazu Kanegane*, Koichi Tsuneyama, Rika Kanezaki, Takeshi Futatani, Keiko Nomura, Shin Ishizawa, Masakiyo Sasahara, Etsuro Ito, Toshio Miyawaki

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

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 β in the severe fibrotic areas of the fibrotic tissues. A real-time polymerase chain reaction (PCR) analysis demonstrated the expression of PDGFα and PDGFβ 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.

Original languageEnglish
Pages (from-to)58-64
Number of pages7
JournalEuropean Journal of Haematology
Volume81
Issue number1
DOIs
StatePublished - 2008/07

Keywords

  • Down syndrome
  • Fibrosis
  • Platelet-derived growth factor
  • Transforming growth factor-β1
  • Transient myeloproliferative disorder

ASJC Scopus subject areas

  • Hematology

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