Base de dados : MEDLINE
Pesquisa : C04.557.470.200.025.085 [Categoria DeCS]
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[PMID]:29287881
[Au] Autor:Ünsaler S; Basaran B; Aslan I; Yilmazbayhan D
[Ad] Endereço:Department of Otolaryngology, Acibadem Altunizade Hospital, Üsküdar, Istanbul, 34662, Turkey. Electronic address: selinunsaler@gmail.com.
[Ti] Título:Endonasal endoscopic nasopharyngectomy for the treatment of nasopharyngeal papillary adenocarcinoma: Report of a rare case.
[So] Source:Int J Pediatr Otorhinolaryngol;104:51-53, 2018 Jan.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:We report a case of low-grade nasopharyngeal papillary adenocarcinoma in a 9 year-old male that was diagnosed incidentally after an adenoidectomy procedure and treated with endonasal endoscopic nasopharyngectomy without any adjuvant therapy. The patient has been followed up for 3 years with no evidence of recurrence. We point out the importance of preoperative fiberoptic nasopharyngoscopy in the absence of longstanding symptoms in school-aged children and histopathologic examination of adenoidectomy specimens in the presence of atypical findings. We also suggest endonasal endoscopic resection in case of papillary adenocarcinoma.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/cirurgia
Carcinoma/cirurgia
Endoscopia/métodos
Neoplasias Nasofaríngeas/cirurgia
Faringectomia/métodos
[Mh] Termos MeSH secundário: Adenoidectomia
Criança
Seres Humanos
Masculino
Procedimentos Cirúrgicos Nasais/métodos
Nariz/patologia
Nariz/cirurgia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180309
[Lr] Data última revisão:
180309
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171231
[St] Status:MEDLINE


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[PMID]:29381996
[Au] Autor:Zhang WL; Ma S; Havrilla L; Cai L; Yu CQ; Shen S; Xu HT; Wang L; Yu JH; Lin XY; Wang E; Yang LH
[Ad] Endereço:Department of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University.
[Ti] Título:Primary thyroid-like low-grade nasopharyngeal papillary adenocarcinoma: A case report and literature review.
[So] Source:Medicine (Baltimore);96(47):e8851, 2017 Nov.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Primary thyroid-like low-grade nasopharyngeal papillary adenocarcinoma (TL-LGNPPA) is an extremely rare malignant nasopharyngeal tumor with features resembling papillary thyroid carcinoma including nuclear positive expression of thyroid transcription factor-1 (TTF-1). PATIENT CONCERNS: A 64-year-old male presented with nasal bleeding and a foreign body sensation of the nasopharynx. Laryngoscopy revealed a 2.0-cm broad-based mass with a smooth surface on the posterior wall of the nasopharynx. A biopsy was obtained. DIAGNOSES: Histopathologic examination demonstrated tumor cells arranged in both papillary and glandular architecture. The tumor cells express nuclear immunoreactivity for TTF-1. The diagnosis of TL-LGNPPA was made. INTERVENTIONS: After the patient was diagnosed with TL-LGNPPA, he underwent complete surgical resection. OUTCOMES: There was no recurrence or evidence of metastatic disease at the 12-month follow-up. LESSONS: TL-LGNPPA is easy to misdiagnose as metastatic papillary thyroid carcinoma or other relative primary adenocarcinomas. It is important to have a broad differential diagnosis and know the key features of each entity because the prognosis and clinical treatment of each may differ.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/patologia
Neoplasias Nasofaríngeas/patologia
[Mh] Termos MeSH secundário: Adenocarcinoma Papilar/diagnóstico
Carcinoma Papilar/diagnóstico
Diagnóstico Diferencial
Seres Humanos
Imuno-Histoquímica
Masculino
Meia-Idade
Neoplasias Nasofaríngeas/diagnóstico
Nasofaringe/patologia
Neoplasias da Glândula Tireoide/diagnóstico
Fator Nuclear 1 de Tireoide/metabolismo
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Thyroid Nuclear Factor 1)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180209
[Lr] Data última revisão:
180209
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180201
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008851


  3 / 3562 MEDLINE  
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[PMID]:28550497
[Au] Autor:Fukumura Y; Nakanuma Y; Kakuda Y; Takase M; Yao T
[Ad] Endereço:Department of Human Pathology, School of Medicine, Juntendo University, Hongo 2-1-1, Tokyo, 113-8421, Japan. yfuku@juntendo.ac.jp.
[Ti] Título:Clinicopathological features of intraductal papillary neoplasms of the bile duct: a comparison with intraductal papillary mucinous neoplasm of the pancreas with reference to subtypes.
[So] Source:Virchows Arch;471(1):65-76, 2017 Jul.
[Is] ISSN:1432-2307
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Intraductal papillary epithelial neoplasms of the pancreatobiliary system (intraductal papillary neoplasm of the bile duct (IPNB) and intraductal papillary mucinous neoplasm (IPMN)) seem to share many clinicopathological features; however, IPNB has not been fully characterized. In order to understand the clinicopathological/immunohistochemical features of IPNB better, we compared 52 cases of IPNB with 42 cases of IPMNs with mural nodules. The IPNB cases were divided into two groups according to their histological similarity and according to five key histological findings. All IPNB and IPMN cases mainly affected middle-aged to elderly people, predominantly men. Mucin hypersecretion was less frequent in IPNB compared to IPMN. Group 2 IPNB more frequently had a higher histopathological grade and more extensive stromal invasion than IPMN. Group 1 IPNB and IPMN were further classified into four subtypes (gastric, intestinal, pancreatobiliary, and oncocytic). Although each subtype of IPNB and IPMN showed similar histology, the immunohistochemical results were different. The gastric type of IPNB was less frequently positive for CDX2, and intestinal IPNB was more frequently positive for MUC1 and less frequently positive for MUC2, MUC5AC, and CDX2 compared to each subtype of IPMN, respectively. In conclusion, IPNB and IPMN have some clinicopathological features in common, but mucin hypersecretion was less frequent both in IPNBs than in IPMN. Group 2 IPNB differed from IPMN in several parameters of tumor aggressiveness. Additional clinicopathological and molecular studies should be performed with respect to the subtypes of IPNB and IPMN.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/patologia
Neoplasias dos Ductos Biliares/patologia
Biomarcadores Tumorais/análise
[Mh] Termos MeSH secundário: Adenocarcinoma Mucinoso/patologia
Idoso
Carcinoma Ductal Pancreático/patologia
Feminino
Seres Humanos
Imuno-Histoquímica
Masculino
Meia-Idade
Neoplasias Pancreáticas/patologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Biomarkers, Tumor)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:171006
[Lr] Data última revisão:
171006
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170528
[St] Status:MEDLINE
[do] DOI:10.1007/s00428-017-2144-9


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[PMID]:28495496
[Au] Autor:Weingertner N; Gressel A; Battistella M; Cribier B
[Ad] Endereço:Department of Pathology, Strasbourg University Hospital, Strasbourg, France. Electronic address: noelle.weingertner@chru-strasbourg.fr.
[Ti] Título:Aggressive digital papillary adenocarcinoma: A clinicopathological study of 19 cases.
[So] Source:J Am Acad Dermatol;77(3):549-558.e1, 2017 Sep.
[Is] ISSN:1097-6787
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Aggressive digital papillary adenocarcinomas (ADPA) are malignant tumors of sweat glands having recurrence/metastatic potential. OBJECTIVE: We sought to describe the clinical/histopathological characteristics of a series of ADPA. METHODS: This is a retrospective case series of 19 ADPA. RESULTS: The tumors occurred in 17 men and 2 women (mean age: 47 years). They involved digits (15), big toe (3), and palm (1), and measured from 3 to 30 mm. They were mostly solid and cystic, with papillary projections and tubular structures. Atypia was mostly mild to moderate. Tumors tested positive for p63, keratin 7, keratin 77 (eccrine duct-specific), PHLDA1, and epithelial membrane antigen in most cases, and for carcinoembryonic antigen, smooth muscle actin, S100 protein, estrogen, progesterone, and androgen receptors in 50%. Mean Ki67 proliferation index was 15%. Local recurrence was observed in 4 cases. One patient had axillary lymph node metastasis. Histopathologic parameters were not predictive of evolution. Conservative surgical treatment, performed in 7 of 19 cases, did not result in more recurrences than amputation. LIMITATIONS: The study was retrospective and the number of cases is small. CONCLUSION: ADPA are histologically variable, but papillary projections are always present. Keratin 77 expression suggests an eccrine origin. P63 is helpful to exclude metastasis. Conservative surgery may be sufficient in some cases.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/patologia
Neoplasias das Glândulas Sudoríparas/patologia
[Mh] Termos MeSH secundário: Adulto
Feminino
Seres Humanos
Masculino
Meia-Idade
Estudos Retrospectivos
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170907
[Lr] Data última revisão:
170907
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170513
[St] Status:MEDLINE


  5 / 3562 MEDLINE  
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[PMID]:28381386
[Au] Autor:Park JR; Li F; Oza VM; Sklaw BC; Cronley KM; Wellner M; Swanson B; Krishna SG
[Ad] Endereço:Division of Hospital Medicine, Division of Gastroenterology, Hepatology and Nutrition, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA. Somashekar_krishna@osumc.edu.
[Ti] Título:High-grade pancreatic intraepithelial lesions: prevalence and implications in pancreatic neoplasia.
[So] Source:Hepatobiliary Pancreat Dis Int;16(2):202-208, 2017 Apr.
[Is] ISSN:1499-3872
[Cp] País de publicação:Singapore
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: High-grade pancreatic intraepithelial neoplasia (PanIN-3), a precursor of pancreatic ductal adenocarcinoma (PDAC), is not universally detected in resected pancreatic neoplasms. We sought to determine the prevalence and prognostic relevance of PanIN-3 lesions in primary surgical resections of PDACs and intraductal papillary mucinous neoplasms (IPMNs). METHODS: A retrospective review of a tertiary care center pathology database (1/2000-6/2014) was performed. Demographics, imaging, pathology, disease-recurrence, and survival data were reviewed. RESULTS: A total of 458 patients who underwent primary pancreatic resection were included. "PanIN-3" lesions were found in 74 (16.2%) patients who either had PDAC (n=67) or main duct (MD)-IPMN (n=7). Among IPMN-MDs, PanIN-3 lesions were exclusively found in those with pathological evidence of chronic pancreatitis. For PDACs, the median overall survival (OS) for pancreata with PanIN-3 lesions was significantly better than those without (OS 1.12 years, inter-quartile range [IQR] 0.72, 2.05 years vs OS 0.86 years, IQR 0.64, 1.60 years respectively; P=0.04). Multivariate Cox regression analysis demonstrated that the presence of PanIN-3 lesions was associated with a reduced risk of death (HR=0.43; 95% CI: 0.23-0.82; P=0.01). CONCLUSIONS: Following primary resection of pancreatic adenocarcinoma, the lower survival observed in patients without PanIN-3 lesions might suggest a state of complete or accelerated transformation. Further investigations are necessary to validate these findings that might impact disease prognosis and management.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/patologia
Carcinoma in Situ/patologia
Carcinoma Ductal Pancreático/patologia
Neoplasias Císticas, Mucinosas e Serosas/patologia
Neoplasias Pancreáticas/patologia
[Mh] Termos MeSH secundário: Adenocarcinoma Papilar/mortalidade
Adenocarcinoma Papilar/cirurgia
Idoso
Carcinoma in Situ/mortalidade
Carcinoma in Situ/cirurgia
Carcinoma Ductal Pancreático/mortalidade
Carcinoma Ductal Pancreático/cirurgia
Distribuição de Qui-Quadrado
Bases de Dados Factuais
Feminino
Seres Humanos
Estimativa de Kaplan-Meier
Masculino
Meia-Idade
Análise Multivariada
Gradação de Tumores
Recidiva Local de Neoplasia
Neoplasias Císticas, Mucinosas e Serosas/mortalidade
Neoplasias Císticas, Mucinosas e Serosas/cirurgia
Ohio
Pancreatectomia
Neoplasias Pancreáticas/mortalidade
Neoplasias Pancreáticas/cirurgia
Modelos de Riscos Proporcionais
Estudos Retrospectivos
Fatores de Risco
Centros de Atenção Terciária
Fatores de Tempo
Resultado do Tratamento
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171023
[Lr] Data última revisão:
171023
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170407
[St] Status:MEDLINE


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[PMID]:28373443
[Au] Autor:Oku Y; Nishiya N; Tsuda K; Shibazaki M; Maesawa C; Uehara Y
[Ad] Endereço:Departments of Integrated Information for Pharmaceutical Sciences, Iwate Medical University School of Pharmacy, Iwate, Japan yoku@iwate-med.ac.jp.
[Ti] Título:Dynamic Phenotypic Transition of Breast Cancer Cells Revealed by Self-floating Cell Culture.
[So] Source:Anticancer Res;37(4):1793-1797, 2017 04.
[Is] ISSN:1791-7530
[Cp] País de publicação:Greece
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Breast tumor heterogeneity leads to phenotypic diversity, such as tumor-initiating and metastatic properties and drug sensitivity. MATERIALS AND METHODS: We found that a self-floating cell (SFC) culture enriches a drug-resistant subpopulation in a HER2-positive breast cancer cell line. SFCs were analyzed for cancer stem cell markers, gene expression profiles, and sensitivity for anticancer drugs. RESULTS: SFCs expressed cancer stem cell markers, such as aldehyde dehydrogenase (ALDH) activity and elevated HER2 autophosphorylation. Gene expression profiles of SFCs showed a dramatic difference compared to those of parental or forced floating cells. SFCs also expressed CD133, a marker of drug resistance, and resisted cytotoxic drugs by drug efflux transporters. In contrast, HER2 kinase inhibitors efficiently reduced SFC viability. CONCLUSION: SFCs enrich drug-resistant subpopulations even in vitro and might reflect the highly plastic nature of breast cancer cells even in vitro.
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/patologia
Adenocarcinoma/patologia
Neoplasias da Mama/patologia
Técnicas de Cultura de Células/métodos
Células-Tronco Neoplásicas/patologia
[Mh] Termos MeSH secundário: Adenocarcinoma/tratamento farmacológico
Adenocarcinoma/genética
Adenocarcinoma/metabolismo
Adenocarcinoma Papilar/tratamento farmacológico
Adenocarcinoma Papilar/genética
Adenocarcinoma Papilar/metabolismo
Aldeído Desidrogenase/genética
Aldeído Desidrogenase/metabolismo
Antineoplásicos/farmacologia
Biomarcadores Tumorais/genética
Biomarcadores Tumorais/metabolismo
Western Blotting
Neoplasias da Mama/tratamento farmacológico
Neoplasias da Mama/genética
Neoplasias da Mama/metabolismo
Proliferação Celular/efeitos dos fármacos
Sobrevivência Celular/efeitos dos fármacos
Resistência a Medicamentos Antineoplásicos/genética
Feminino
Citometria de Fluxo
Sequenciamento de Nucleotídeos em Larga Escala
Seres Humanos
Técnicas In Vitro
Células-Tronco Neoplásicas/efeitos dos fármacos
Células-Tronco Neoplásicas/metabolismo
Fenótipo
Células Tumorais Cultivadas
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antineoplastic Agents); 0 (Biomarkers, Tumor); EC 1.2.1.3 (Aldehyde Dehydrogenase)
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170413
[Lr] Data última revisão:
170413
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170405
[St] Status:MEDLINE


  7 / 3562 MEDLINE  
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[PMID]:28299799
[Au] Autor:Patel K; Wu H; Pimpalwar A; Diwan AH
[Ad] Endereço:Department of Pathology, Texas Children's Hospital, Houston, Texas.
[Ti] Título:Response to: Cutaneous papillary adenocarcinoma in situ.
[So] Source:J Cutan Pathol;44(6):598-599, 2017 06.
[Is] ISSN:1600-0560
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Adenocarcinoma Papilar
Neoplasias Cutâneas
[Mh] Termos MeSH secundário: Adenocarcinoma
Seres Humanos
[Pt] Tipo de publicação:LETTER; COMMENT
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170317
[St] Status:MEDLINE
[do] DOI:10.1111/cup.12919


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[PMID]:28282455
[Au] Autor:Carlson GE; Martin EW; Shirure VS; Malgor R; Resto VA; Goetz DJ; Burdick MM
[Ad] Endereço:Department of Chemical and Biomolecular Engineering, Russ College of Engineering and Technology, Ohio University, Athens, Ohio, United States of America.
[Ti] Título:Dynamic biochemical tissue analysis detects functional L-selectin ligands on colon cancer tissues.
[So] Source:PLoS One;12(3):e0173747, 2017.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:A growing body of evidence suggests that L-selectin ligands presented on circulating tumor cells facilitate metastasis by binding L-selectin presented on leukocytes. Commonly used methods for detecting L-selectin ligands on tissues, e.g., immunostaining, are performed under static, no-flow conditions. However, such analysis does not assay for functional L-selectin ligands, specifically those ligands that promote adhesion under shear flow conditions. Recently our lab developed a method, termed dynamic biochemical tissue analysis (DBTA), to detect functional selectin ligands in situ by probing tissues with L-selectin-coated microspheres under hemodynamic flow conditions. In this investigation, DBTA was used to probe human colon tissues for L-selectin ligand activity. The detection of L-selectin ligands using DBTA was highly specific. Furthermore, DBTA reproducibly detected functional L-selectin ligands on diseased, e.g., cancerous or inflamed, tissues but not on noncancerous tissues. In addition, DBTA revealed a heterogeneous distribution of functional L-selectin ligands on colon cancer tissues. Most notably, detection of L-selectin ligands by immunostaining using HECA-452 antibody only partially correlated with functional L-selectin ligands detected by DBTA. In summation, the results of this study demonstrate that DBTA detects functional selectin ligands to provide a unique characterization of pathological tissue.
[Mh] Termos MeSH primário: Bioquímica/métodos
Neoplasias do Colo/metabolismo
Selectina L/metabolismo
[Mh] Termos MeSH secundário: Adenocarcinoma Mucinoso/metabolismo
Adenocarcinoma Mucinoso/patologia
Adenocarcinoma Papilar/metabolismo
Adenocarcinoma Papilar/patologia
Carcinoma de Células em Anel de Sinete/metabolismo
Carcinoma de Células em Anel de Sinete/patologia
Neoplasias do Colo/patologia
Formaldeído
Glicoconjugados/análise
Glicoconjugados/metabolismo
Seres Humanos
Ligantes
Microscopia de Fluorescência
Microesferas
Fixação de Tecidos/métodos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Glycoconjugates); 0 (Ligands); 126880-86-2 (L-Selectin); 1HG84L3525 (Formaldehyde)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170311
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0173747


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[PMID]:28244498
[Au] Autor:Crippa S; Pezzilli R; Bissolati M; Capurso G; Romano L; Brunori MP; Calculli L; Tamburrino D; Piccioli A; Ruffo G; Fave GD; Falconi M
[Ad] Endereço:Department of Surgery, Sacro Cuore-Don Calabria Hospital, Negrar, Verona, Italy.
[Ti] Título:Active Surveillance Beyond 5 Years Is Required for Presumed Branch-Duct Intraductal Papillary Mucinous Neoplasms Undergoing Non-Operative Management.
[So] Source:Am J Gastroenterol;112(7):1153-1161, 2017 Jul.
[Is] ISSN:1572-0241
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: To evaluate the results of active surveillance beyond 5 years in patients with branch-duct intraductal papillary mucinous neoplasms (BD-IPMNs) without worrisome features (WF) and high-risk stigmata (HRS) undergoing non-operative management. METHODS: Patients with a minimum follow-up of 5 years who underwent surveillance with at least yearly magnetic resonance imaging were included. New onset of and predictors of WF/HRS during follow-up as well as long-term survival were analyzed. RESULTS: In all, 144 patients were followed for a median of 84 months. At diagnosis multifocal BD-IPMNs were found in 53% of cases and mean size of the largest cyst was 15.5 mm. Changes during follow-up were observed in 69 patients (48%). New onset of WF/HRS were observed in 26 patients (18%) but the rate of HRS was only 4%. WF and HRS developed after a median follow-up of 71 and 77.5 months from diagnosis, respectively, and without previous changes in 19/26 patients. Independent predictors of WF/HRS development were size at diagnosis>15 mm, increase in number of lesions, main pancreatic duct growth rate ≥0.2 mm/year, cyst growth rate >1 mm/year. Overall, the rate of pancreatic invasive malignancy was 2% and the 12-year disease-specific survival was 98.6%. CONCLUSIONS: Long-term nonoperative management is safe for BD-IPMNs without WF and HRS. Discontinuation of surveillance cannot be recommended since one out of six patients developed WF/HRS far beyond 5 years of surveillance and without previous relevant modifications. An intensification of follow-up should be considered after 5 years.
[Mh] Termos MeSH primário: Adenocarcinoma Mucinoso/patologia
Adenocarcinoma Mucinoso/terapia
Adenocarcinoma Papilar/patologia
Adenocarcinoma Papilar/terapia
Carcinoma Ductal Pancreático/patologia
Carcinoma Ductal Pancreático/terapia
Ductos Pancreáticos/patologia
Neoplasias Pancreáticas/patologia
Neoplasias Pancreáticas/terapia
Vigilância da População
[Mh] Termos MeSH secundário: Biópsia por Agulha Fina
Colangiopancreatografia por Ressonância Magnética
Progressão da Doença
Endossonografia
Feminino
Seres Humanos
Itália
Imagem por Ressonância Magnética
Masculino
Meia-Idade
Prognóstico
Fatores de Tempo
[Pt] Tipo de publicação:JOURNAL ARTICLE; MULTICENTER STUDY
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170301
[St] Status:MEDLINE
[do] DOI:10.1038/ajg.2017.43


  10 / 3562 MEDLINE  
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[PMID]:28195111
[Au] Autor:Kar A; Kar T; Dha I; Panda S
[Ad] Endereço:Department of Pathology, S.C.B. Medical College, Cuttack, Odisha, India.
[Ti] Título:Squash cytodiagnosis of synchronous papillary serous carcinoma of ovary and endometrium with demonstration of serous tubal intraepithelial carcinoma as a precursor lesion.
[So] Source:Indian J Pathol Microbiol;60(1):125-127, 2017 Jan-Mar.
[Is] ISSN:0974-5130
[Cp] País de publicação:India
[La] Idioma:eng
[Mh] Termos MeSH primário: Adenocarcinoma Papilar/diagnóstico
Carcinoma in Situ/diagnóstico
Cistadenocarcinoma Seroso/diagnóstico
Citodiagnóstico
Neoplasias do Endométrio/diagnóstico
Neoplasias Ovarianas/diagnóstico
[Mh] Termos MeSH secundário: Adenocarcinoma Papilar/complicações
Adenocarcinoma Papilar/patologia
Biomarcadores Tumorais/análise
Carcinoma in Situ/complicações
Carcinoma in Situ/patologia
Cistadenocarcinoma Seroso/complicações
Cistadenocarcinoma Seroso/patologia
Neoplasias do Endométrio/complicações
Neoplasias do Endométrio/patologia
Endométrio/patologia
Feminino
Histocitoquímica
Seres Humanos
Imuno-Histoquímica
Antígeno Ki-67/análise
Microscopia
Meia-Idade
Neoplasias Ovarianas/complicações
Neoplasias Ovarianas/patologia
Ovário/patologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Biomarkers, Tumor); 0 (Ki-67 Antigen)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170620
[Lr] Data última revisão:
170620
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170215
[St] Status:MEDLINE
[do] DOI:10.4103/0377-4929.200039



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