Volume 41, Issue 4 pp. 334-337

PANCREATOBLASTOMA

Three original cases and review of the literature

E. Kohda

E. Kohda

Departments of Radiology,

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M. IsekiH. IkawaM. EndohJ. YokoyamaM. Mukai

M. Mukai

Pathology, Keio University School of Medicine, and Departments of

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J. Hata

J. Hata

Pathology, Keio University School of Medicine, and Departments of

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H. Yamazaki

H. Yamazaki

Departments of Radiology,

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J. Miyauchi

J. Miyauchi

Pathology and

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M. Saeki

M. Saeki

Surgery, The National Children Hospital, Tokyo, Japan

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Correspondence:Ehiichi Kohda, Department of Radiology, Keio University School of Medicine, Shinanomachi 35, Shinjuku-ku, Tokyo 160, Japan. FAX +81 3 3353 1977.

Abstract

Purpose: To describe the characteristics of pancreatoblastoma.

Material and Methods: We studied 3 cases of pancretoblastoma and reviewed another 59 cases. Parameters analyzed were tumor site, hemorrhage, capsule formation, necrosis, vascularity, production of alpha-fetoprotein (AFP), cystic changes and calcification.

Results: The diagnostic findings were as follows: pancreatic head origin (24/54, 44%), pancreatic body and tail origin (30/54, 56%), hemorrhage (16/17, 94%), capsule formation (24/26, 92%), necrosis (28/31, 90%), hypervascularity (10/14, 71%), production of AFP (19/28, 68%), cystic changes (11/16, 69%), and calcification (10/21, 48%). All neonatal cases demonstrated cystic changes. Three of them were patients with Beckwith-Wiedmann syndrome. The incidence of capsule formation and calcification was not related to the origin of the tumor.

Conclusion: The most common features of pancreatoblastoma are hemorrhage, capsule formation and necrosis.

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