Publication: A multihormonal tumor of the pancreas producing neurotensin associated with the WDHA syndrome. Histology, histochemistry and origin
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Date
1986
Authors
Bani-Sacchi, Tatiana ; Bartolini, Giancarlo ; Biliotti, Giancarlo
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
A pancreatic tumor associated with severe
LVDHA syndrome has been studied histologically and
immunohistochemically. Light microscopy revealed that
the growth pattern of' the tunlor varied greatly from zone
to zone but with prevailing solid arrangement of the
tumoral cells. The majority of the endocrine cells showed
numerous eosinophilic, PTAH-positive, and argyrophilic
secretory granules, that were ultrastructurally similar to
those of normal and tumoral neurotensin-containing cells.
A minority of the endocrine cells had secretory granules
ultrastructurally different from the aforementioned ones,
but these were not diagnostic on purely morphological
grounds.
Inside the tumor, immunol~istochemistryd emonstrated
a majority of neurotensin-immunoreactive cells, sparse
and small clusters of VIP-immunoreactive cells and few,
dispersed pancreatic polypeptide-immunoreactive cells.
Some structural and ultrastructural aspects of the
tumoral stroma have also been reported.
Ducts and solid masses of duct-like cells were also
found, and small clusters and singly dispersed duct-like
cells were seen invading the endocrine tissue and undergoing
mitoses. Such features suggest that the tumor
originated from precursors located in the medium-sized
and small pancreatic ducts.
Because of the multihormonal nature of the tumor, the
role of neurotensin and VIP in producing the patient's
symptoms is discussed and a synergistic action of the two
hormones is suggested in causing the particularly severe
WDHA syndrome.
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