Solid pseudopapillary neoplasm of the pancreas: Clinical-pathological features and management, a single-center experience

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Solid pseudopapillary neoplasm of the pancreas : Clinical-pathological features and management, a single-center experience. / Hansen, Carsten Palnaes; Kristensen, Thomas Skaarup; Storkholm, Jan Henrik; Federspiel, Birgitte Hartnack.

I: Rare Tumors, Bind 11, 01.2019, s. 1-8.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hansen, CP, Kristensen, TS, Storkholm, JH & Federspiel, BH 2019, 'Solid pseudopapillary neoplasm of the pancreas: Clinical-pathological features and management, a single-center experience', Rare Tumors, bind 11, s. 1-8. https://doi.org/10.1177/2036361319878513

APA

Hansen, C. P., Kristensen, T. S., Storkholm, J. H., & Federspiel, B. H. (2019). Solid pseudopapillary neoplasm of the pancreas: Clinical-pathological features and management, a single-center experience. Rare Tumors, 11, 1-8. https://doi.org/10.1177/2036361319878513

Vancouver

Hansen CP, Kristensen TS, Storkholm JH, Federspiel BH. Solid pseudopapillary neoplasm of the pancreas: Clinical-pathological features and management, a single-center experience. Rare Tumors. 2019 jan.;11:1-8. https://doi.org/10.1177/2036361319878513

Author

Hansen, Carsten Palnaes ; Kristensen, Thomas Skaarup ; Storkholm, Jan Henrik ; Federspiel, Birgitte Hartnack. / Solid pseudopapillary neoplasm of the pancreas : Clinical-pathological features and management, a single-center experience. I: Rare Tumors. 2019 ; Bind 11. s. 1-8.

Bibtex

@article{f414572b74884ea8ad74acf6a51f9b7b,
title = "Solid pseudopapillary neoplasm of the pancreas: Clinical-pathological features and management, a single-center experience",
abstract = "Solid pseudopapillary neoplasm of the pancreas is a rare tumor of low malignancy that occurs most often in females. The study describes the clinicopathologic characteristics of the tumor and common differential diagnoses. Data were collected from a prospectively maintained database. Of 1661 patients operated for pancreatic tumors between January 2001 and September 2018, 15 patients were recorded. Patients included 12 females and 3 males, median age 40 (range 10 -87) years. Computed tomography or magnetic resonance imaging was diagnostic in eight patients and a preoperative biopsy in eight out of 10 patients. Median tumor size was 5 cm (range 2 -16 cm), 12 tumors were in the head, six in the body, and three in the tail of the gland. All patients except one had radical resection including one with hepatic and lymph node metastases, no patient underwent oncologic treatment. All patients are alive from 17.5 to 209.4 months postoperatively and without recurrence. Radical operation is usually curative and should also be offered to patients with metastases or recurrence as oncologic treatment has limited effect.",
keywords = "histology, immunohistochemistry, Pancreas, solid pseudopapillary neoplasm, treatment",
author = "Hansen, {Carsten Palnaes} and Kristensen, {Thomas Skaarup} and Storkholm, {Jan Henrik} and Federspiel, {Birgitte Hartnack}",
year = "2019",
month = jan,
doi = "10.1177/2036361319878513",
language = "English",
volume = "11",
pages = "1--8",
journal = "Rare Tumors",
issn = "2036-3605",
publisher = "Pagepress",

}

RIS

TY - JOUR

T1 - Solid pseudopapillary neoplasm of the pancreas

T2 - Clinical-pathological features and management, a single-center experience

AU - Hansen, Carsten Palnaes

AU - Kristensen, Thomas Skaarup

AU - Storkholm, Jan Henrik

AU - Federspiel, Birgitte Hartnack

PY - 2019/1

Y1 - 2019/1

N2 - Solid pseudopapillary neoplasm of the pancreas is a rare tumor of low malignancy that occurs most often in females. The study describes the clinicopathologic characteristics of the tumor and common differential diagnoses. Data were collected from a prospectively maintained database. Of 1661 patients operated for pancreatic tumors between January 2001 and September 2018, 15 patients were recorded. Patients included 12 females and 3 males, median age 40 (range 10 -87) years. Computed tomography or magnetic resonance imaging was diagnostic in eight patients and a preoperative biopsy in eight out of 10 patients. Median tumor size was 5 cm (range 2 -16 cm), 12 tumors were in the head, six in the body, and three in the tail of the gland. All patients except one had radical resection including one with hepatic and lymph node metastases, no patient underwent oncologic treatment. All patients are alive from 17.5 to 209.4 months postoperatively and without recurrence. Radical operation is usually curative and should also be offered to patients with metastases or recurrence as oncologic treatment has limited effect.

AB - Solid pseudopapillary neoplasm of the pancreas is a rare tumor of low malignancy that occurs most often in females. The study describes the clinicopathologic characteristics of the tumor and common differential diagnoses. Data were collected from a prospectively maintained database. Of 1661 patients operated for pancreatic tumors between January 2001 and September 2018, 15 patients were recorded. Patients included 12 females and 3 males, median age 40 (range 10 -87) years. Computed tomography or magnetic resonance imaging was diagnostic in eight patients and a preoperative biopsy in eight out of 10 patients. Median tumor size was 5 cm (range 2 -16 cm), 12 tumors were in the head, six in the body, and three in the tail of the gland. All patients except one had radical resection including one with hepatic and lymph node metastases, no patient underwent oncologic treatment. All patients are alive from 17.5 to 209.4 months postoperatively and without recurrence. Radical operation is usually curative and should also be offered to patients with metastases or recurrence as oncologic treatment has limited effect.

KW - histology

KW - immunohistochemistry

KW - Pancreas

KW - solid pseudopapillary neoplasm

KW - treatment

U2 - 10.1177/2036361319878513

DO - 10.1177/2036361319878513

M3 - Journal article

C2 - 31598207

AN - SCOPUS:85073319451

VL - 11

SP - 1

EP - 8

JO - Rare Tumors

JF - Rare Tumors

SN - 2036-3605

ER -

ID: 241104715