Chromosome 22q11 deletion complicated by dissecting pulmonary arterial aneurysm and jejunal atresia in an infant

Shoji Yamanaka, Yukichi Tanaka, Motoyoshi Kawataki, Rieko Ijiri, Kiyoshi Imaizumi, Hiroki Kurahashi

研究成果: Article査読

9 被引用数 (Scopus)

抄録

We present an autopsy case of a 46-day-old male infant with chromosome 22q11 deletion, which is considered the primary cause of several diseases, including DiGeorge syndrome and velocardiofacial syndrome. The patient had 2 notable congenital abnormalities: multiple dissecting pulmonary arterial aneurysms distributed in both lungs and multiple jejunal atresia with apple- peel deformity. The former, a very rare pathologic condition especially in infancy, was found incidentally at autopsy and was the primary cause of death. To our knowledge, neither of these lesions has been reported previously in a patient with chromosome 22q11 deletion.

本文言語English
ページ(範囲)880-882
ページ数3
ジャーナルArchives of Pathology and Laboratory Medicine
124
6
出版ステータスPublished - 2000
外部発表はい

ASJC Scopus subject areas

  • 病理学および法医学
  • 医療検査技術

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