Volume 20, Issue 5 pp. 633-639
Original Article

Living donor domino liver transplantation using a maple syrup urine disease donor: A case series of three children – The first report from Japan

Masatoshi Matsunami

Corresponding Author

Masatoshi Matsunami

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

Masatoshi Matsunami, Organ Transplantation Center, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan

Tel.: +81 3 3416 0181

Fax: +81 3 3416-2222

E-mail: [email protected]

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Akinari Fukuda

Akinari Fukuda

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Kengo Sasaki

Kengo Sasaki

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Hajime Uchida

Hajime Uchida

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Takanobu Shigeta

Takanobu Shigeta

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Yoshihiro Hirata

Yoshihiro Hirata

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Hiroyuki Kanazawa

Hiroyuki Kanazawa

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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Reiko Horikawa

Reiko Horikawa

Division of Endocrinology and Metabolism, National Center for Child Health and Development, Tokyo, Japan

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Atsuko Nakazawa

Atsuko Nakazawa

Division of Clinical Pathology, National Center for Child Health and Development, Tokyo, Japan

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Tatsuya Suzuki

Tatsuya Suzuki

Department of Pediatric Surgery, Fujita Health University School of Medicine, Aichi, Japan

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Koichi Mizuta

Koichi Mizuta

Department of Transplant Surgery, Jichi Medical University, Tochigi, Japan

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Mureo Kasahara

Mureo Kasahara

Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan

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First published: 08 February 2016
Citations: 16

Abstract

As the priority of LD-Domino LT is the safety of the first recipient, limitations and technical difficulties in the second recipient often occur. The most technically challenging part of LD-Domino LT is the reconstruction of the vessels. For the reconstruction of HVs, the native HVs were exteriorized as far as possible using a CUSA because longer extensive HVs are essential for facilitating the reconstruction. At the back table, the HVs of the domino graft were sutured together, and the single cuff of the HVs was anastomosed to the IVC by joining the orifices. The HAs, the presence of insufficient length, and multiple vessels in the whole liver rendered the reconstruction more difficult. We determined the dividing sites of the vessels according to the preoperative 3D-CT findings obtained in two institutions. This is the first case series using grafts in DLT obtained from LDLT for patients with MSUD between two institutions. In conclusion, LD-Domino LT is a safe and feasible therapeutic option to expand the donor pool by technical refinement in the reconstruction of the second recipient. Further studies with a greater accumulation of patients and a longer follow-up will be necessary to establish LD-Domino LT using an MSUD donor.

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