Pathological findings in dicephalus dipus dibrachius : implications for mechanisms in two pairs of lateral conjoined twins

• ITOH K.

  Department of Pathology, Kobe University School of Medicine

• Imai Y

  Department of Pathology, Kobe University School of Medicine

• Obayashi C

  Department of Pathology, Kobe University School of Medicine

• Hayashi Y

  Department of Pathology, Kobe University School of Medicine

• Hanioka K

  Department of Pathology, Kobe University School of Medicine

• Itoh H

  Department of Pathology, Kobe University School of Medicine

抄録

The anatomical and pathological features of two pairs of dicephalic conjoined twins (case 1 and 2) are described. Both twins showed duplicitas lateralis representing diprosopus dipus dibrachius. There were two complete heads on two necks, one thorax, one abdomen and externally normal two arms and two legs. Case 1 showed dicephalus with anencephaly, two vertebral columns and two spinal cords, which converged from the thoracic region distally. The esophagus, stomachs and partial small intestines were duplicated, which fused at yolk sac (with Meckel's diverticulum). The heart was incompletely fused. The lungs and trachea were doubled. Two spinal cords were fused from the thoracic region caudally and showed myelomeningocele and Arnold-Chiari malformation in case 2. Two larynxes and two thracheas connected with the incompletely fused three lobes of lungs. The conjoined lungs were hypoplastic. The heart was single, showing ventral septal defect, transposition of great arteries, two cuspid aortic valves and preductal aortic coarctation. The duplicated esophagi were conjoined in Y-shape and single stomach, duodenum, intestine and colon were found. There were pairs of kidneys, adrenal glands and ureters and single female genitalia in both cases. These findings indicate that the craniocaudal paleoaxes were separated in the cranial region and converted or fused under the thoracic region like a Y-shape. Further development defects and deformations might be important factors to form malformations in these case.

収録刊行物

• Kobe J. Med. Sci.

  Kobe J. Med. Sci. 39 95-106, 1993

  神戸大学

詳細情報

• CRID: 1571980077503622528
• NII論文ID: 110007000209
• NII書誌ID: AA00711740
• ISSN: 00232513
• 本文言語コード: en
• データソース種別:
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