Primary squamous cell carcinoma of the ampulla of Vater: a case report

Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-...
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Autor*in:	Balci, B. [verfasserIn] Calik, B. Karadeniz, T. Sahin, H. Ugurlu, L. Aydin, C.

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2016

Schlagwörter:	Ampulla of Vater Squamous cell carcinoma

Anmerkung:	© Balci et al. 2016

Übergeordnetes Werk:	Enthalten in: Surgical case reports - Berlin : SpringerOpen, 2015, 2(2016), 1 vom: 08. Jan.
Übergeordnetes Werk:	volume:2 ; year:2016 ; number:1 ; day:08 ; month:01

Links:	Volltext

DOI / URN:	10.1186/s40792-016-0130-0

Katalog-ID:	SPR037751514

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520			\|a Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor.
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allfields	10.1186/s40792-016-0130-0 doi (DE-627)SPR037751514 (SPR)s40792-016-0130-0-e DE-627 ger DE-627 rakwb eng Balci, B. verfasserin aut Primary squamous cell carcinoma of the ampulla of Vater: a case report 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Balci et al. 2016 Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213 Calik, B. aut Karadeniz, T. aut Sahin, H. aut Ugurlu, L. aut Aydin, C. aut Enthalten in Surgical case reports Berlin : SpringerOpen, 2015 2(2016), 1 vom: 08. Jan. (DE-627)818040475 (DE-600)2809613-7 2198-7793 nnns volume:2 year:2016 number:1 day:08 month:01 https://dx.doi.org/10.1186/s40792-016-0130-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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 2 2016 1 08 01
spelling	10.1186/s40792-016-0130-0 doi (DE-627)SPR037751514 (SPR)s40792-016-0130-0-e DE-627 ger DE-627 rakwb eng Balci, B. verfasserin aut Primary squamous cell carcinoma of the ampulla of Vater: a case report 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Balci et al. 2016 Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213 Calik, B. aut Karadeniz, T. aut Sahin, H. aut Ugurlu, L. aut Aydin, C. aut Enthalten in Surgical case reports Berlin : SpringerOpen, 2015 2(2016), 1 vom: 08. Jan. (DE-627)818040475 (DE-600)2809613-7 2198-7793 nnns volume:2 year:2016 number:1 day:08 month:01 https://dx.doi.org/10.1186/s40792-016-0130-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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 2 2016 1 08 01
allfields_unstemmed	10.1186/s40792-016-0130-0 doi (DE-627)SPR037751514 (SPR)s40792-016-0130-0-e DE-627 ger DE-627 rakwb eng Balci, B. verfasserin aut Primary squamous cell carcinoma of the ampulla of Vater: a case report 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Balci et al. 2016 Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213 Calik, B. aut Karadeniz, T. aut Sahin, H. aut Ugurlu, L. aut Aydin, C. aut Enthalten in Surgical case reports Berlin : SpringerOpen, 2015 2(2016), 1 vom: 08. Jan. (DE-627)818040475 (DE-600)2809613-7 2198-7793 nnns volume:2 year:2016 number:1 day:08 month:01 https://dx.doi.org/10.1186/s40792-016-0130-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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 2 2016 1 08 01
allfieldsGer	10.1186/s40792-016-0130-0 doi (DE-627)SPR037751514 (SPR)s40792-016-0130-0-e DE-627 ger DE-627 rakwb eng Balci, B. verfasserin aut Primary squamous cell carcinoma of the ampulla of Vater: a case report 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Balci et al. 2016 Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213 Calik, B. aut Karadeniz, T. aut Sahin, H. aut Ugurlu, L. aut Aydin, C. aut Enthalten in Surgical case reports Berlin : SpringerOpen, 2015 2(2016), 1 vom: 08. Jan. (DE-627)818040475 (DE-600)2809613-7 2198-7793 nnns volume:2 year:2016 number:1 day:08 month:01 https://dx.doi.org/10.1186/s40792-016-0130-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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 2 2016 1 08 01
allfieldsSound	10.1186/s40792-016-0130-0 doi (DE-627)SPR037751514 (SPR)s40792-016-0130-0-e DE-627 ger DE-627 rakwb eng Balci, B. verfasserin aut Primary squamous cell carcinoma of the ampulla of Vater: a case report 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Balci et al. 2016 Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213 Calik, B. aut Karadeniz, T. aut Sahin, H. aut Ugurlu, L. aut Aydin, C. aut Enthalten in Surgical case reports Berlin : SpringerOpen, 2015 2(2016), 1 vom: 08. Jan. (DE-627)818040475 (DE-600)2809613-7 2198-7793 nnns volume:2 year:2016 number:1 day:08 month:01 https://dx.doi.org/10.1186/s40792-016-0130-0 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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 2 2016 1 08 01
language	English
source	Enthalten in Surgical case reports 2(2016), 1 vom: 08. Jan. volume:2 year:2016 number:1 day:08 month:01
sourceStr	Enthalten in Surgical case reports 2(2016), 1 vom: 08. Jan. volume:2 year:2016 number:1 day:08 month:01
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institution	findex.gbv.de
topic_facet	Ampulla of Vater Squamous cell carcinoma
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authorswithroles_txt_mv	Balci, B. @@aut@@ Calik, B. @@aut@@ Karadeniz, T. @@aut@@ Sahin, H. @@aut@@ Ugurlu, L. @@aut@@ Aydin, C. @@aut@@
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author	Balci, B.
spellingShingle	Balci, B. misc Ampulla of Vater misc Squamous cell carcinoma Primary squamous cell carcinoma of the ampulla of Vater: a case report
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topic_title	Primary squamous cell carcinoma of the ampulla of Vater: a case report Ampulla of Vater (dpeaa)DE-He213 Squamous cell carcinoma (dpeaa)DE-He213
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title	Primary squamous cell carcinoma of the ampulla of Vater: a case report
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title_full	Primary squamous cell carcinoma of the ampulla of Vater: a case report
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title_sort	primary squamous cell carcinoma of the ampulla of vater: a case report
title_auth	Primary squamous cell carcinoma of the ampulla of Vater: a case report
abstract	Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. © Balci et al. 2016
abstractGer	Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. © Balci et al. 2016
abstract_unstemmed	Background Primary squamous cell carcinoma of the ampulla of Vater is a very rare type of tumor, and the prognosis is not well known mainly due to a limited number of cases reported. Here, we aimed to report a case with primary squamous cell carcinoma of the ampulla of Vater. Case presentation A 54-year-old woman presented with weight loss, jaundice, and pain in the epigastric and right upper quadrant of the abdomen. With extensive radiological imaging, the patient was diagnosed with periampullary tumor and Whipple’s procedure was performed. The immunohistochemical analyses supported the diagnosis of primary squamous cell carcinoma. The postoperative course was uneventful. The patient was discharged, and adjuvant chemotherapy was recommended. Conclusion Primary squamous cell carcinoma of the ampulla of Vater is a very rare histological type with an unclear pathogenesis. A better understanding of pathogenesis might be helpful in optimizing the treatment for this specific rare type of tumor. © Balci et al. 2016
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title_short	Primary squamous cell carcinoma of the ampulla of Vater: a case report
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author2	Calik, B. Karadeniz, T. Sahin, H. Ugurlu, L. Aydin, C.
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