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1.
Ann Ital Chir ; 72(1): 89-92; discussion 92-3, 2001.
Artículo en Italiano | MEDLINE | ID: mdl-11464502

RESUMEN

Gastric carcinoid is a rare disease, representing less than 1% of gastric tumours and 11-41% of all gastrointestinal carcinoids. The recent Solcia's classification distinguishes three subtypes of these neoplasms, which show specific clinical and pathological features. Type one arises in patients with chronic atrophic gastritis (CGA), achlorhydria, hypergastrinemia and consequent enterochromaffin-like cell hyperplasia and dysplasia. Type two is related to Zollinger Ellison syndrome and type three represents the sporadic kind. We report two cases of multifocal gastric carcinoid associated to CGA, one of them with pernicious anemia. Both patients had aspecific abdominal symptoms; the diagnosis was suspected by upper endoscopy and confirmed by histological examination. Patients were submitted to total gastrectomy. They are still alive six years after surgery, without signs or symptoms of recurrences. Treatment of these tumours is controversial, because of their uncertain biological and clinical behaviour. Some Authors propose a conservative strategy (only endoscopic surveillance or removal); others stress importance of surgery (antrectomy or gastric resection). We discuss and underline the role of surgical therapy and the relevance of radical approach.


Asunto(s)
Tumor Carcinoide/complicaciones , Gastritis Atrófica/complicaciones , Neoplasias Gástricas/complicaciones , Adulto , Anciano , Tumor Carcinoide/patología , Femenino , Gastritis Atrófica/clasificación , Gastritis Atrófica/patología , Humanos , Neoplasias Gástricas/patología
2.
Ann Ital Chir ; 72(1): 67-72, 2001.
Artículo en Italiano | MEDLINE | ID: mdl-11464499

RESUMEN

The aim of present study was to assess preoperative/postoperative serum gastrin level variations and their prognostic value in patients with colo-rectal cancer. Levels have been evaluated in 66 subjects undergoing colo-rectal cancer surgery, with curative intent, from may 1990 to february 1994. Preoperative gastrin analysis was performed on peripheral blood samples in starred patient just prior surgery. Postoperative gastrin assessment was performed 7 day after surgery in starred patients as well. Follow-up ranged from 5 to 8 years. No association between preoperative gastrin levels and tumor site, stage or grading was observed. No significant variation of preoperative gastrin levels (p > 0.05) was ascertained postoperatively neither in the whole patient series nor after correction for tumor stage. Postoperative levels were therefore not affected by surgical removal of cancer. Neither preoperative nor postoperative serum gastrin levels influenced significantly the 5-year survival. In our experience, with the limitation of a small series assessment, serum gastrin level do not seem to have any prognostic value in colo-rectal cancer.


Asunto(s)
Neoplasias Colorrectales/sangre , Gastrinas/sangre , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Cuidados Posoperatorios , Cuidados Preoperatorios , Pronóstico
3.
Ann Ital Chir ; 72(2): 221-5, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11552478

RESUMEN

Our previous experimental data demonstrated that a new gastrin receptor antagonist (CR2945) has a chemopreventive effect on dimethylhydrazine-induced colon cancer in mice. The aim of this study is to test the effect of CR2945 on the appearance and distribution of aberrant crypt foci (ACF), proposed as early "preneoplastic" lesions in colon carcinogenesis, in the murine model. 176 CD1 male mice were randomly divided into 4 groups: group 1, sham group received 2 daily intra-peritoneal injections of saline solution; group 2 received 1 weekly intra-peritoneal injection of DMH 20 mg/kg, for 5 weeks, and 2 daily intra-peritoneal injections of equal volume of NaCl 0.9%; group 3 and 4 received the same weekly dose of DMH and 2 daily injections of CR2945 at the respective doses of 2.5 and 7.5 mg/Kg for 5 weeks. The rodents were sacrified 15, 20, 25, and 38 weeks after receiving the first injection. The number of ACF per area (ACF frequency), their multiplicity (number of crypts per focus), ACF frequency according to each colonic site were recorded. No ACF were found in the sham group. No substantial differences were observed in ACF distribution between the remaining groups. Our hypothesis is that CR2945 does not alter the final number of ACF but might induce a regression of some dysplastic ACF.


Asunto(s)
Benzodiazepinas/farmacología , Colon/patología , Receptores de Colecistoquinina/antagonistas & inhibidores , 1,2-Dimetilhidrazina , Animales , Carcinógenos , Colon/efectos de los fármacos , Neoplasias del Colon/patología , Masculino , Ratones
4.
Eur Surg Res ; 31(3): 272-80, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10352356

RESUMEN

Previous studies are consistent with the hypothesis that aberrant crypt foci (ACF) could be intermediate biomarkers in colorectal carcinogenesis. The present controlled experimental trial was performed to sequentially analyze ACF progression in rat colonic mucosa. F344 rats were administered 2-weekly doses of azoxymethane (15 mg/kg body weight, s.c.) and sacrificed 6, 12, 20, 30 and 36 weeks after the first carcinogen injection. Control groups of untreated rats were sacrificed at the same time points. The number of ACF per area, their multiplicity (number of crypts per focus), ACF frequency and multiplicity according to each colonic site, histology of ACF and macroscopic lesions were recorded. No ACF were found in control animals. In treated animals, the number of ACF per area and the multiplicity progressively and significantly increased throughout the study. ACF were prevalent in the mid colon. Lower frequencies were registered in the distal colon and rectum. ACF were rare in the proximal colon and cecum. By histology, ACF presented superficial and extensive hyperplasia. Tumors were found in the 30th and 36th week. Adenomas and well-differentiated adenocarcinomas were in the distal colon. All proximal neoplasms were signet ring cell carcinomas. In our study, ACF growing features and distribution are not correlated to adenoma and adenocarcinoma distribution. It is conceivable that signet ring cell carcinomas arising in the proximal colon, where ACF are rare, could present a different pathway of growth. The preneoplastic role of ACF and their function as intermediate biomarkers in colorectal carcinogenesis remain to be clarified.


Asunto(s)
Neoplasias Colorrectales/patología , Lesiones Precancerosas/patología , Adenocarcinoma/inducido químicamente , Adenocarcinoma/patología , Adenoma/inducido químicamente , Adenoma/patología , Animales , Azoximetano , Carcinoma de Células en Anillo de Sello/inducido químicamente , Carcinoma de Células en Anillo de Sello/patología , División Celular , Neoplasias Colorrectales/inducido químicamente , Hiperplasia/inducido químicamente , Hiperplasia/patología , Mucosa Intestinal/efectos de los fármacos , Mucosa Intestinal/patología , Masculino , Lesiones Precancerosas/inducido químicamente , Ratas , Ratas Endogámicas F344
5.
Digestion ; 65(1): 35-40, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-11961341

RESUMEN

BACKGROUND/AIMS: The potential role of gastrin and the cholecystokinin-B (CCK-B)/gastrin receptor in the genesis of colon cancer is debated. Aberrant crypt foci (ACF) are considered to be preneoplastic lesions of colon cancer. We aimed to assess whether the CCK-B/gastrin receptor antagonist, CR2945, may prevent the development of ACF and adenocarcinoma in the experimental model of dimethylhydrazine (DMH)-induced colorectal cancer. MATERIALS AND METHODS: 226 CD1 mice were randomized into 3 groups (sham, control and treated) and received intraperitoneal injections of NaCl 0.9%, DMH, and DMH + CR2945, respectively, for 5 weeks. 168 mice were sacrificed at 15, 38, 45 and 52 weeks after the first injection day. The colon and rectum were investigated for frequency, multiplicity and distribution of ACF as well as for adenocarcinoma at histology. The expression of gastrin was assessed in tumor samples at histology by immunohistochemistry. RESULTS: ACF frequency and multiplicity significantly increased with time in both controls and treated mice with no difference between groups except that at week 45. 38.8% of controls and 14.3% of treated mice developed cancer (p = 0.004). No cancer was positive for gastrin at immunohistochemistry. The mean number of cancers per mouse and the proportion of mice with cancer increased with time with statistically significant difference between controls and treated mice at week 38 only but not afterwards. A significant correlation between cancer and ACF frequency (r = 0.35) and multiplicity (r = 0.25) was observed. CONCLUSIONS: Our findings support the preneoplastic significance of ACF and indicate that CR2945 treatment does not interfere with the DMH-induced carcinogenic process.


Asunto(s)
Adenocarcinoma/prevención & control , Benzodiazepinas/farmacología , Neoplasias del Colon/prevención & control , Receptores de Colecistoquinina/antagonistas & inhibidores , Adenocarcinoma/inducido químicamente , Animales , Neoplasias del Colon/inducido químicamente , Masculino , Ratones , Ratones Endogámicos , Receptor de Colecistoquinina B , Factores de Tiempo
6.
Eur Surg Res ; 31(5): 406-11, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10529554

RESUMEN

This study tested the effect of a new gastrin receptor antagonist, CR2945, on colorectal cancer induced by 1,2-dimethylhydrazine (DMH) in mice. 75 CD1 male mice were divided into 3 groups: group 1 received 1 weekly injection of 20 mg/kg of DMH and 2 daily intraperitoneal injections of 0.5 ml of NaCl 0.9% solution for 5 weeks; groups 2 and 3 received the same weekly dose of DMH and 2 daily injections of CR2945 at the respective doses of 2.5 and 7.5 mg/kg for 5 weeks. The animals were sacrificed 25 and 38 weeks after the first injection. No tumours were found at the 25th week. A lower cancer frequency (4%) was observed in treated animals compared to controls (37.4%) at the 38th week (p = 0.002). These data show that CR2945 could prevent chemically induced colon cancer development in mice.


Asunto(s)
1,2-Dimetilhidrazina , Benzodiazepinas/farmacología , Carcinógenos , Neoplasias Colorrectales/inducido químicamente , Neoplasias Colorrectales/prevención & control , Receptores de Colecistoquinina/antagonistas & inhibidores , Adenocarcinoma/inducido químicamente , Adenocarcinoma/epidemiología , Adenocarcinoma/patología , Adenocarcinoma/prevención & control , Adenoma/inducido químicamente , Adenoma/epidemiología , Adenoma/patología , Adenoma/prevención & control , Animales , Neoplasias Colorrectales/epidemiología , Neoplasias Colorrectales/patología , Incidencia , Masculino , Ratones , Ratones Endogámicos
7.
Br J Cancer ; 88(3): 401-5, 2003 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-12569383

RESUMEN

Various histologic classification systems have been proposed as prognostic factors for gastric cancer. We assessed the prognostic value of Goseki classification as well as the TNM staging system, histological tumour grading, Lauren, WHO, Goseki and Siewert classifications in 100 patients with cardia carcinoma undergoing curative surgery. Two patients were lost at follow-up. The median time of follow-up in the remaining patients was 32.9 months after surgery (range: 0.1-142.1 months). No differences in survival rates were observed according to tumour grading, Lauren or WHO histologic or Siewert topographical classification. No differences were found according to Goseki classes, when considering either the mucin content of the carcinoma (types I and III vs II and IV) or the differentiation grade (types I and II vs III and IV). Multivariate analysis showed that the only lymph node positivity was a significant predictor of survival: 7.2% of patients with, but 41.5% of those without nodal involvement were alive after five years (P=0.0001). In conclusion, we found no prognostic role for Goseki or the traditional histological indexes, while the TNM staging system and particularly lymph node positivity were the main predictors of survival in patients with cardia adenocarcinoma.


Asunto(s)
Adenocarcinoma/patología , Neoplasias Cardíacas/patología , Adenocarcinoma/mortalidad , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Neoplasias Cardíacas/mortalidad , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Análisis de Supervivencia
9.
Rev. argent. dermatol ; 78(4): 238-40, oct. 1997. ilus
Artículo en Español | LILACS | ID: lil-221061

RESUMEN

Presentamos un caso de neurofibromatosis tipo I, diagnosticado a partir de una consulta por vitiligo en una niña de nueve años de edad


Asunto(s)
Humanos , Femenino , Neurofibromatosis/clasificación , Neurofibromatosis/diagnóstico , Manifestaciones Cutáneas , Manifestaciones Oculares
10.
Rev. argent. dermatol ; 81(4): 212-5, oct.-dic. 2000. graf
Artículo en Español | LILACS | ID: lil-278352

RESUMEN

Los autores estudian los cambios observados en las internacions de pacientes con UMI dutante el período 1995-1998 en el Hospital Carrasco, con especial referncia a egresos, tiempo de estadía, costos de internación y reinternaciones.Exponen protocolo de internacxión para estos pacientes, haciéndose referencia también a los problemas sociales que estas patologías determinan


Asunto(s)
Humanos , Protocolos Clínicos , Costo de Enfermedad , Costos de Hospital/estadística & datos numéricos , Úlcera de la Pierna/epidemiología , Úlcera de la Pierna/psicología , Tiempo de Internación/estadística & datos numéricos
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