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Successful treatment of metastatic pancreatoblastoma in an adult with autologous hematopoietic cell transplant.

作者信息

Elghawy Omar, Wang John S, Whitehair Rachel M, Grosh William, Kindwall-Keller Tamila L

机构信息

School of Medicine, University of Virginia, Charlottesville, VA, USA.

University of Virginia, Department of Pathology, Charlottesville, VA, USA.

出版信息

Pancreatology. 2021 Jan;21(1):188-191. doi: 10.1016/j.pan.2020.10.049. Epub 2020 Nov 2.

Abstract

BACKGROUND

Pancreatoblastoma is a rare pediatric malignant neoplasm characterized by its histological resemblance to fetal pancreatic tissue and poor clinical outcomes. Preoperative diagnosis of the neoplasm is difficult due to its rarity, variable clinical presentation, and its lack of distinct laboratory markers. Current mainstay of treatment is surgical resection of the tumor, although a standard of care has not yet been established.

METHODS

Data were collected on one patient admitted to the University of Virginia Hospital System. Radiology, hematopoietic cell transplant, and biopsy data were collected according to the best clinical practice.

RESULTS

Herein, we describe the case of an adult patient with pancreatoblastoma treated with high-dose chemotherapy and autologous peripheral blood hematopoietic cell transplantation. To the authors' knowledge, this is the first documented successful treatment of pancreatoblastoma using autologous hematopoietic cell transplantation in the United States, and the first successful treatment in an adult patient worldwide.

CONCLUSIONS

While it is difficult to draw conclusions based on a single case, we would like to highlight the success of this treatment modality in the management of our patient with a 51-month remission and open further discussion into exploring the use of autologous hematopoietic cell transplantation for pancreatoblastoma. Our patient is currently living 57 months after diagnosis despite the average survival rate being less than 18 months.

摘要

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