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Heterotopic pancreas--clinical presentation and pathology with review of the literature.

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Heterotopic pancreas--clinical presentation and pathology with review of the literature. / Eisenberger, C F; Gocht, Andreas; Knoefel, W T; Busch, C B; Peiper, M; Kutup, A; Yekebas, E F; Hosch, S B; Lambrecht, W; Izbicki, J R.

In: HEPATO-GASTROENTEROL, Vol. 51, No. 57, 57, 2004, p. 854-858.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Eisenberger, CF, Gocht, A, Knoefel, WT, Busch, CB, Peiper, M, Kutup, A, Yekebas, EF, Hosch, SB, Lambrecht, W & Izbicki, JR 2004, 'Heterotopic pancreas--clinical presentation and pathology with review of the literature.', HEPATO-GASTROENTEROL, vol. 51, no. 57, 57, pp. 854-858. <http://www.ncbi.nlm.nih.gov/pubmed/15143933?dopt=Citation>

APA

Eisenberger, C. F., Gocht, A., Knoefel, W. T., Busch, C. B., Peiper, M., Kutup, A., Yekebas, E. F., Hosch, S. B., Lambrecht, W., & Izbicki, J. R. (2004). Heterotopic pancreas--clinical presentation and pathology with review of the literature. HEPATO-GASTROENTEROL, 51(57), 854-858. [57]. http://www.ncbi.nlm.nih.gov/pubmed/15143933?dopt=Citation

Vancouver

Eisenberger CF, Gocht A, Knoefel WT, Busch CB, Peiper M, Kutup A et al. Heterotopic pancreas--clinical presentation and pathology with review of the literature. HEPATO-GASTROENTEROL. 2004;51(57):854-858. 57.

Bibtex

@article{b88d30c1301d42d6ac67ea241377750b,
title = "Heterotopic pancreas--clinical presentation and pathology with review of the literature.",
abstract = "BACKGROUND/AIMS: Heterotopic pancreas is usually a silent gastrointestinal malformation, but it may become clinically evident when complicated by chronic inflammation or by growth. METHODOLOGY: We report on eleven cases of heterotopic pancreatic tissue. The cases were selected from the records of our Surgical Department and Institute of Pathology. The literature about heterotopic pancreas is reviewed. RESULTS: Nausea and vomiting (27%), epigastric pain (27%), ulceration (27%) and weight loss (18%) were the three most frequent symptoms and signs. The lesions were diagnosed as gastrointestinal tumor or ulcer by gastroduodenoscopy (36%). The other patients were diagnosed during surgery (64%). Definitive diagnosis was only achievable by pathology. Heterotopic pancreas was the reason for surgery in 36% of the cases, in another 45% diagnosis was incidental during surgery and in 18% the diagnosis was established endoscopically and surgery was not necessary. CONCLUSIONS: The diagnosis of heterotopic pancreas is rarely established, most cases remain clinically silent. In symptomatic patients diagnosis should to be secured histologically to exclude malignant disease.",
author = "Eisenberger, {C F} and Andreas Gocht and Knoefel, {W T} and Busch, {C B} and M Peiper and A Kutup and Yekebas, {E F} and Hosch, {S B} and W Lambrecht and Izbicki, {J R}",
year = "2004",
language = "Deutsch",
volume = "51",
pages = "854--858",
number = "57",

}

RIS

TY - JOUR

T1 - Heterotopic pancreas--clinical presentation and pathology with review of the literature.

AU - Eisenberger, C F

AU - Gocht, Andreas

AU - Knoefel, W T

AU - Busch, C B

AU - Peiper, M

AU - Kutup, A

AU - Yekebas, E F

AU - Hosch, S B

AU - Lambrecht, W

AU - Izbicki, J R

PY - 2004

Y1 - 2004

N2 - BACKGROUND/AIMS: Heterotopic pancreas is usually a silent gastrointestinal malformation, but it may become clinically evident when complicated by chronic inflammation or by growth. METHODOLOGY: We report on eleven cases of heterotopic pancreatic tissue. The cases were selected from the records of our Surgical Department and Institute of Pathology. The literature about heterotopic pancreas is reviewed. RESULTS: Nausea and vomiting (27%), epigastric pain (27%), ulceration (27%) and weight loss (18%) were the three most frequent symptoms and signs. The lesions were diagnosed as gastrointestinal tumor or ulcer by gastroduodenoscopy (36%). The other patients were diagnosed during surgery (64%). Definitive diagnosis was only achievable by pathology. Heterotopic pancreas was the reason for surgery in 36% of the cases, in another 45% diagnosis was incidental during surgery and in 18% the diagnosis was established endoscopically and surgery was not necessary. CONCLUSIONS: The diagnosis of heterotopic pancreas is rarely established, most cases remain clinically silent. In symptomatic patients diagnosis should to be secured histologically to exclude malignant disease.

AB - BACKGROUND/AIMS: Heterotopic pancreas is usually a silent gastrointestinal malformation, but it may become clinically evident when complicated by chronic inflammation or by growth. METHODOLOGY: We report on eleven cases of heterotopic pancreatic tissue. The cases were selected from the records of our Surgical Department and Institute of Pathology. The literature about heterotopic pancreas is reviewed. RESULTS: Nausea and vomiting (27%), epigastric pain (27%), ulceration (27%) and weight loss (18%) were the three most frequent symptoms and signs. The lesions were diagnosed as gastrointestinal tumor or ulcer by gastroduodenoscopy (36%). The other patients were diagnosed during surgery (64%). Definitive diagnosis was only achievable by pathology. Heterotopic pancreas was the reason for surgery in 36% of the cases, in another 45% diagnosis was incidental during surgery and in 18% the diagnosis was established endoscopically and surgery was not necessary. CONCLUSIONS: The diagnosis of heterotopic pancreas is rarely established, most cases remain clinically silent. In symptomatic patients diagnosis should to be secured histologically to exclude malignant disease.

M3 - SCORING: Zeitschriftenaufsatz

VL - 51

SP - 854

EP - 858

IS - 57

M1 - 57

ER -