Malignant carcinoid tumor of the pancreas

Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells. Carcinoid tumor of the pancreas is a very rare tumor with less than 50 cases reported in world literature. In literature it is denoted &q...
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Autor*in:	Čolović Radoje B. [verfasserIn] Micev Marjan [verfasserIn] Čolović Nataša [verfasserIn] Zogović Sergej [verfasserIn] Trbojević Božo J. [verfasserIn] Stojković Mirjana [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch ; srp

Erschienen:	2002

Schlagwörter:	pancreas malignant carcinoid Whipple's procedure

Übergeordnetes Werk:	In: Srpski Arhiv za Celokupno Lekarstvo - Serbian Medical Society, 2010, 130(2002), 5-6, Seite 204-207
Übergeordnetes Werk:	volume:130 ; year:2002 ; number:5-6 ; pages:204-207

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.2298/SARH0206204C

Katalog-ID:	DOAJ013778757

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spelling	10.2298/SARH0206204C doi (DE-627)DOAJ013778757 (DE-599)DOAJaa62395d865a42799352017edb7cb337 DE-627 ger DE-627 rakwb eng srp Čolović Radoje B. verfasserin aut Malignant carcinoid tumor of the pancreas 2002 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells. Carcinoid tumor of the pancreas is a very rare tumor with less than 50 cases reported in world literature. In literature it is denoted "pancreatic serotoninoma" or "serotonin-producing pancreatic tumor". Due to its rarity the tumor is an unusual cause of carcinoid syndrome. As the carcinoid tumor of the pancreas does not always causes carcinoid syndrome its absence does not necessarily exclude the existence of the tumor. The tumor is frequently malignant. Over 50% of patients have metastases at the time of surgery. This is the reason why radical surgery is not possible in a number of patients. Excisional surgery offers the best chance for recovery or long term survival. We report on a 57-year-old woman with carcinoid syndrome caused by malignant carcinoid tumor of the head of the pancreas without liver or other distant metastases; it was successfully excised with pylorus preserving cephalic duo-denopancreatectomy (after Longmire-Traverso) and radical lymphadenectomy. The diagnosis was established on the basis of histologic and immunohistochemical findings. The patient is symptom free for more than eight months. pancreas malignant carcinoid Whipple's procedure Medicine R Micev Marjan verfasserin aut Čolović Nataša verfasserin aut Zogović Sergej verfasserin aut Trbojević Božo J. verfasserin aut Stojković Mirjana verfasserin aut In Srpski Arhiv za Celokupno Lekarstvo Serbian Medical Society, 2010 130(2002), 5-6, Seite 204-207 (DE-627)637421205 (DE-600)2577665-4 24060895 nnns volume:130 year:2002 number:5-6 pages:204-207 https://doi.org/10.2298/SARH0206204C kostenfrei https://doaj.org/article/aa62395d865a42799352017edb7cb337 kostenfrei http://www.doiserbia.nb.rs/img/doi/0370-8179/2002/0370-81790206204C.pdf kostenfrei https://doaj.org/toc/0370-8179 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 130 2002 5-6 204-207
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author	Čolović Radoje B.
spellingShingle	Čolović Radoje B. misc pancreas misc malignant carcinoid misc Whipple's procedure misc Medicine misc R Malignant carcinoid tumor of the pancreas
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topic_title	Malignant carcinoid tumor of the pancreas pancreas malignant carcinoid Whipple's procedure
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title	Malignant carcinoid tumor of the pancreas
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title_full	Malignant carcinoid tumor of the pancreas
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author_browse	Čolović Radoje B. Micev Marjan Čolović Nataša Zogović Sergej Trbojević Božo J. Stojković Mirjana
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title_sort	malignant carcinoid tumor of the pancreas
title_auth	Malignant carcinoid tumor of the pancreas
abstract	Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells. Carcinoid tumor of the pancreas is a very rare tumor with less than 50 cases reported in world literature. In literature it is denoted "pancreatic serotoninoma" or "serotonin-producing pancreatic tumor". Due to its rarity the tumor is an unusual cause of carcinoid syndrome. As the carcinoid tumor of the pancreas does not always causes carcinoid syndrome its absence does not necessarily exclude the existence of the tumor. The tumor is frequently malignant. Over 50% of patients have metastases at the time of surgery. This is the reason why radical surgery is not possible in a number of patients. Excisional surgery offers the best chance for recovery or long term survival. We report on a 57-year-old woman with carcinoid syndrome caused by malignant carcinoid tumor of the head of the pancreas without liver or other distant metastases; it was successfully excised with pylorus preserving cephalic duo-denopancreatectomy (after Longmire-Traverso) and radical lymphadenectomy. The diagnosis was established on the basis of histologic and immunohistochemical findings. The patient is symptom free for more than eight months.
abstractGer	Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells. Carcinoid tumor of the pancreas is a very rare tumor with less than 50 cases reported in world literature. In literature it is denoted "pancreatic serotoninoma" or "serotonin-producing pancreatic tumor". Due to its rarity the tumor is an unusual cause of carcinoid syndrome. As the carcinoid tumor of the pancreas does not always causes carcinoid syndrome its absence does not necessarily exclude the existence of the tumor. The tumor is frequently malignant. Over 50% of patients have metastases at the time of surgery. This is the reason why radical surgery is not possible in a number of patients. Excisional surgery offers the best chance for recovery or long term survival. We report on a 57-year-old woman with carcinoid syndrome caused by malignant carcinoid tumor of the head of the pancreas without liver or other distant metastases; it was successfully excised with pylorus preserving cephalic duo-denopancreatectomy (after Longmire-Traverso) and radical lymphadenectomy. The diagnosis was established on the basis of histologic and immunohistochemical findings. The patient is symptom free for more than eight months.
abstract_unstemmed	Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells. Carcinoid tumor of the pancreas is a very rare tumor with less than 50 cases reported in world literature. In literature it is denoted "pancreatic serotoninoma" or "serotonin-producing pancreatic tumor". Due to its rarity the tumor is an unusual cause of carcinoid syndrome. As the carcinoid tumor of the pancreas does not always causes carcinoid syndrome its absence does not necessarily exclude the existence of the tumor. The tumor is frequently malignant. Over 50% of patients have metastases at the time of surgery. This is the reason why radical surgery is not possible in a number of patients. Excisional surgery offers the best chance for recovery or long term survival. We report on a 57-year-old woman with carcinoid syndrome caused by malignant carcinoid tumor of the head of the pancreas without liver or other distant metastases; it was successfully excised with pylorus preserving cephalic duo-denopancreatectomy (after Longmire-Traverso) and radical lymphadenectomy. The diagnosis was established on the basis of histologic and immunohistochemical findings. The patient is symptom free for more than eight months.
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title_short	Malignant carcinoid tumor of the pancreas
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Malignant carcinoid tumor of the pancreas

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