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1.
Oncol Lett ; 3(1): 16-18, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22740848

RESUMO

Tumour growth involves two essential deviations from the normal state including the induction of proliferative stimuli, and simultaneous suppression of potentially compensatory cell death. It has been suggested that the development of invasive cancer involves a progressive switch from predominantly apoptotic to necrotic tumour cell death. The presence of tumour necrosis in pathologic specimens may not only reflect tumour biology, but also provide additional beneficial prognostic information. This review emphasises the role of tumour necrosis as an additional prognostic factor for patients with certain types of epithelial neoplasms.

2.
Ultrastruct Pathol ; 36(3): 139-44, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22455876

RESUMO

Inflammatory cell infiltration around the sites of carcinoma invasion is believed to play important roles in tumor biological behavior. The status of inflammatory cell infiltration at the sites of frank invasion in 92 cases of gastric carcinomas was examined, with special emphasis on tumor-associated tissue eosinophilia (TATE). TATE was found in 7 out of 92 (7.6%) gastric carcinomas (6 of intestinal-type and 1 of diffuse-type). Electron microscopy, selectively performed in the 7 cases of gastric carcinomas with TATE, showed that eosinophils participated in the stromal reaction by interacting with tumor cells, mast cells, and each other. Most of the tumor-infiltrating mast cells exhibited anaphylactic or piecemeal degranulation, indicating that the mast cells had been activated in situ. Some mast cells were noted in close contact to viable tumor cells, suggesting the existence of direct cell-to-cell interactions. There was also extracellular deposition of free eosinophil granules and Charcot-Leyden crystals. These morphologic findings are similar to that described in late/chronic-phase allergic reaction in both human and experimental animals, where angiogenesis and fibrosis/tissue repair are also present. In conclusion, TATE may indicate a chronic allergic-like Th2 host-tumor reaction, and understanding these pathways should create tools to enhance defence and contrast neoplastic disease.


Assuntos
Adenocarcinoma/ultraestrutura , Hipersensibilidade/patologia , Inflamação/patologia , Neoplasias Gástricas/ultraestrutura , Células Estromais/ultraestrutura , Adenocarcinoma/imunologia , Adenocarcinoma/cirurgia , Idoso , Degranulação Celular , Doença Crônica , Cristalização , Eosinofilia/imunologia , Eosinofilia/patologia , Eosinófilos/imunologia , Eosinófilos/ultraestrutura , Feminino , Humanos , Hipersensibilidade/imunologia , Inflamação/imunologia , Masculino , Mastócitos/imunologia , Mastócitos/ultraestrutura , Pessoa de Meia-Idade , Neoplasias Gástricas/imunologia , Neoplasias Gástricas/cirurgia , Células Estromais/imunologia
3.
Ultrastruct Pathol ; 35(4): 145-9, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21657821

RESUMO

A histological variant of gastric adenocarcinoma, characterized by an intense tumor-associated tissue eosinophilia (TATE), has been occasionally reported in the literature. The purpose of this ultrastructural study was to determine the interactions between frequently occurring eosinophils and tumor cells in gastric carcinoma characterized by TATE. Fresh tumor tissue of 92 gastric carcinomas was processed for both light and electron microscopic examination. Intense TATE was found in 7 out of 92 (7.6%) gastric carcinomas (6 of intestinal-type and 1 of diffuse-type). Electron microscopy, selectively performed in 7 cases with intense TATE, revealed eosinophils, singly or in groups, in contact with damaged or necrotic tumor cells. Activated eosinophils showing piecemeal degranulation were also found in intimate contact with viable tumor cells, characterized by plasma membrane caveolar invaginations. The authors regard this close morphological relationship as in vivo evidence for possible cross-talk between eosinophil and viable tumor cell, a conclusion that has already been drawn from experimental studies, but until now inadequately supported by ultrastructural observations in a human tumor.


Assuntos
Adenocarcinoma/ultraestrutura , Eosinófilos/ultraestrutura , Neoplasias Gástricas/ultraestrutura , Migração Transcelular de Célula/fisiologia , Adenocarcinoma/cirurgia , Idoso , Comunicação Celular/fisiologia , Grânulos Citoplasmáticos/ultraestrutura , Eosinófilos/fisiologia , Feminino , Humanos , Masculino , Microscopia Eletrônica de Transmissão , Pessoa de Meia-Idade , Neoplasias Gástricas/cirurgia
4.
Ultrastruct Pathol ; 35(2): 66-71, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21299346

RESUMO

Mitotic catastrophe is a common phenomenon occurring in tumor cells with impaired p53 function exposed to various cytotoxic and genotoxic agents. The defective p53 checkpoint causes improper segregation of chromosomes, resulting in aberrant mitosis, multiple micronuclei, multinucleate giant cells, and eventual necrosis-like death and centrosome aberration. Although various descriptions explaining mitotic catastrophe exist, there is still no generally accepted definition of this phenomenon. However, the syndrome of mitotic catastrophe may be a unifying morphological concept of particular interest to cancer research, as it integrally links cell death to checkpoints of the cell cycle. Morphological findings compatible with mitotic catastrophe may be found in pleomorphic, giant cell carcinomas--neoplasms characterized by a poor prognosis. The inclusion of mitotic catastrophe as part of the microscopic evaluation of tumors will add further insight to the pathobiology of tumor progression and in novel therapeutic designs. Finally, the possibility of assimilating mitotic catastrophe into a prognostic score is discussed.


Assuntos
Carcinoma/patologia , Mitose , Idoso , Carcinoma/química , Carcinoma/ultraestrutura , Morte Celular , Núcleo Celular/patologia , Centrossomo/patologia , Feminino , Humanos , Imuno-Histoquímica , Antígeno Ki-67/análise , Índice Mitótico , Valor Preditivo dos Testes , Prognóstico , Terminologia como Assunto , Proteína Supressora de Tumor p53/análise
5.
Ultrastruct Pathol ; 35(1): 14-8, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20925599

RESUMO

The authors report a case of a 70-year-old woman with an anaplastic giant cell thyroid carcinoma, along with immunohistochemical and electron microscopic findings. Histologically, the tumor is characterized by mononucleated and multinucleated giant cells, lack of architectural cohesion, atypical mitoses, and extensive areas of coagulative necrosis. Tumor cells showed AE1/AE3 positivity as well as nuclear overexpression of p53 and ki-67. Semithin sections revealed multiple nuclei with heterogeneous size ranging from micronuclei to large-size (giant) nuclei. Micronuclei were confirmed by electron microscopy that disclosed also the presence of nuclear blebs, strings, and pockets. Morphological findings of these abnormal nuclear structures in conjunction with p53 and Ki-67 nuclear overexpression suggested a faulty mitotic checkpoint/mitotic catastrophe in the progression of anaplastic giant cell thyroid carcinoma.


Assuntos
Carcinoma de Células Gigantes/ultraestrutura , Núcleo Celular/ultraestrutura , Idoso , Biomarcadores Tumorais/análise , Carcinoma de Células Gigantes/metabolismo , Carcinoma de Células Gigantes/cirurgia , Evolução Fatal , Feminino , Humanos , Imuno-Histoquímica , Metástase Linfática/patologia , Microscopia Eletrônica de Transmissão , Carcinoma Anaplásico da Tireoide , Neoplasias da Glândula Tireoide/metabolismo , Neoplasias da Glândula Tireoide/cirurgia , Neoplasias da Glândula Tireoide/ultraestrutura , Tireoidectomia
6.
Chir Ital ; 56(5): 617-20, 2004.
Artigo em Italiano | MEDLINE | ID: mdl-15553431

RESUMO

From January 1970 to December 1999, 881 patients with thyroid pathology underwent surgery consisting in 551 subtotal thyroidectomies and 330 total thyroidectomies. Permanent hypocalcaemia was present in 32 patients (3.6%). The importance of accurate isolation and ultraligature of the branches of the inferior thyroid artery in the prevention of parathyroid damage is stressed.


Assuntos
Hipocalcemia/etiologia , Hipoparatireoidismo/etiologia , Glândulas Paratireoides/lesões , Tireoidectomia/efeitos adversos , Adulto , Humanos , Fatores de Risco
7.
Chir Ital ; 56(4): 517-21, 2004.
Artigo em Italiano | MEDLINE | ID: mdl-15452990

RESUMO

Adenomas of the rectum are frequently found during endoscopic examination. We report on our 30 years of experience with the treatment of tubulo-villous adenomas based on histotype. Between 1971 and 2001, 104 villous tumours of the rectum were treated surgically. The patients' average age was 65 years. These were sessile tumours in 69% of cases, pedunculated in 17.5% and flowing tumours in 13.5%. The mean tumour size was 3 cm. They were associated with colon cancer in 15% of cases and with polyadenoma in 10%. They were located in the rectum within 0 to 6 cm of the anal margin in half the cases. These tumours were treated by local excision in 74 cases and by wide excision in 30 cases. The malignant potential of the tumours was 30%, including 10% invasive malignancy. There were no surgical fatalities, but a 6% medical fatality rate was registered. There was a 20% complication rate related to the surgical technique. Twenty patients were lost to follow-up. Out of 84 villous tumours, monitored over a mean survival period of 6.5 years, there were 24 recurrences: 18 underwent endoscopic excision and in 6 cases a wide resection. The various tumour resection techniques and the operative indications of variable difficulty are presented. It would seem, at present, that total resection of the rectum with a colo-anal anastomosis is the best treatment for large flowing villous tumours occupying almost the entire rectum. Thorough preoperative examination and the mastering of various surgical procedures should allow the most suitable choice of treatment for each individual case.


Assuntos
Adenoma Viloso/cirurgia , Neoplasias Retais/cirurgia , Adenoma Viloso/diagnóstico , Adenoma Viloso/mortalidade , Adenoma Viloso/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Canal Anal/cirurgia , Anastomose Cirúrgica , Colo/cirurgia , Endoscopia , Seguimentos , Humanos , Pessoa de Meia-Idade , Recidiva Local de Neoplasia , Neoplasias Retais/diagnóstico , Neoplasias Retais/mortalidade , Neoplasias Retais/patologia , Reto/patologia , Fatores de Tempo
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