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. 2016 Nov;50(6):482-485.
doi: 10.4132/jptm.2016.02.27. Epub 2016 May 29.

Goblet Cell Carcinoid of the Rectum in a Patient with Neurofibromatosis Type 1

Affiliations

Goblet Cell Carcinoid of the Rectum in a Patient with Neurofibromatosis Type 1

Youngjin Kang et al. J Pathol Transl Med. 2016 Nov.
No abstract available

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Conflict of interest statement

No potential conflict of interest relevant to this article was reported.

Figures

Fig. 1.
Fig. 1.
The rectum shows a combined occurrence of goblet cell carcinoid (GCC, empty arrows) and neuroendocrine tumors (filled arrows) as well as neurofibromatosis (A). GCC is mostly composed of small nests of signet-ring-like goblet cells (B), and the cytoplasmic mucin is readily identified with alcian blue pH 2.5 (C). (D) Synaptophysin immunostain clearly shows a few scattered neuroendocrine cells in GCC.
Fig. 2.
Fig. 2.
Neuroendocrine tumors (NETs) consist of small uniform cells which exclusively form trabecular structures (A) and diffusely stained with synaptophysin (B). In the vicinity of both goblet cell carcinoid and NETs, proliferation of slender spindle cells morphologically compatible with neurofibromatosis (C) is evident with S-100 protein immunostain (D).
Fig. 3.
Fig. 3.
The submucosal tumor in the jejunum is composed of bland-looking spindle cells (A) which highly expressed c-Kit by immunohistochemistry (B).

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