Abstract |
Pancreatoblastoma is a very rare tumor of the pancreas, affecting children in the first decade of life. Ultrasound and CT scan may be useful but pre-operative diagnosis is often quite difficult. High level of seric alpha-fetoprotein could be suggestive of pancreatoblastoma. The definitive diagnosis is however made by histologists when an organoid structure, well encapsulated, consisting of acinar cells with zymogen-like granules and squamoid corpuscle is demonstrated, sometimes associated with mesenchymal tissue (mixed-type pancreatoblastoma). Immunohistochemical studies may help in differentiating pancreatoblastoma from papillary cystic tumors, acinar cell carcinomas and endocrine pancreatic tumors of the pancreas. We report a case of mixed-type pancreatoblastoma in a 12-year-old female patient, located in the head of the pancreas. The treatment has been surgical, consisting of a duodeno-cephalo-pancreasectomy. Neither radiotherapy nor chemotherapy has been performed. The patient is alive, without recurrence, four months after the operation. Diagnostic, therapeutic and prognostic aspects are discussed.
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Authors | S Latteri, G Russo, R Vecchio, G Meli, F Latteri |
Journal | Minerva chirurgica
(Minerva Chir)
Vol. 51
Issue 9
Pg. 729-35
(Sep 1996)
ISSN: 0026-4733 [Print] Italy |
Vernacular Title | Pancreatoblastoma di tipo misto. Presentazione di un caso clinico. |
PMID | 9082240
(Publication Type: Case Reports, English Abstract, Journal Article)
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Topics |
- Child
- Female
- Humans
- Pancreatic Neoplasms
(pathology)
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