Peritoneal cancer of gynecological origin,

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The aim of this study is a retrospective analysis of the spectrum of ovarian tumors: statistics, epidemiology and pathological features, based on one-year experience in our hospital. Materials and method. We analyzed 58 cases registered in the Peritoneal cancer of gynecological origin Department as oophorectomy or hysterectomy specimens diagnosed with ovarian tumors, including benign, borderline and malignant tumors of various histological types.

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Based on their peritoneal cancer of gynecological origin behavior, we had: three cases of benign tumors, all of them associated with a different histological tumor type and grade in the contralateral ovary, 12 cases of borderline tumors and 46 peritoneal cancer of gynecological origin of malignant tumors 39 cases of primary and 7 cases of secondary tumors.

The most frequent histologic type was represented by high-grade serous carcinoma Rare primary ovarian tumors were represented by: adult granulosa cell tumor, clear cell carcinoma, mixed serous-mucinous carcinoma and undifferentiated pleomorphic sarcoma 1. The earliest age of all patients with ovarian tumors was 31 years old for the mixed serous-mucinous carcinoma.

Mean age distribution was 52 years old for benign tumors, 51 years old for borderline and 60 years old for malignant tumors. Primary malignant tumors are the most frequent type of ovarian tumors and their age incidence ranges from the third to the eighth decade.

The utility of immunohistochemistry in the diagnosis of ovarian carcinoma

The majority of secondary ovarian tumors are of endometrial origin. Keywords ovarian tumors, benign, borderline, malignant Rezumat Obiectiv. Scopul acestui studiu este analiza retrospectivă a spectrului de tumori ovariene, din punct de vedere sta­tis­tic, epidemiologic şi al caracteristicilor histopatologice, re­pre­zen­tând experienţa de un an în spitalul nostru Ma­te­ria­le şi metodă.

Am analizat 58 de cazuri, din De­par­ta­­mentul de Anatomie Patologică, înregistrate ca piese de ooforectomie sau histerectomie diagnosticate cu tumori ovariene, cuprinzând diferite tipuri histologice de tumori ovariene benigne, borderline şi maligne.

În funţie de caracterul tumoral, am identificat: trei cazuri de tumori benigne, toate asociate cu un alt tip histologic tu­moral în ovarul contralateral, 12 cazuri de wart remover on skin tags bor­der­line şi 46 de cazuri de tumori maligne dintre care 39 de cazuri de tumori primare şi 7 cazuri reprezentând tumori secundare. Vârsta minimă în rândul tuturor pacientelor cu tumori ovariene a fost 31 de ani.

Vârsta medie pe categorii a fost 52 de ani pentru tumori benigne, 51 de ani pentru tumori borderline şi 60 de ani pentru tumori maligne. Tumorile maligne primare reprezintă cel mai frecvent tip de tumori ovariene, cu o incidenţă de vârstă cuprinsă între decadele a treia şi a opta de viaţă.

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Majoritatea tumorilor ovariene secundare sunt de origine endometrială. The relative frequency­ of ovarian tumor is different for western and Asian countries. Two third of ovarian tumors occur in women of reproductive age group 1. Borderline tumors occur at slightly older ages and malignant tumors are more common in women between 45 and 65 years old 2.

Studiu clinico-patologic al tumorilor ovariene - experienţa de un an într-un centru medical

Ovarian cancer represents the fifth cause of cancer and the fifth cause of death due to cancer in females in the European Union 3. There are three major histologic subtypes of surface epithelial tumors: serous, mucinous and endometrioid.

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Serous carcinomas are divided in: high-grade serous carcinoma and low-grade serous carcinoma. These tumors are associated with KRAS mutation mainly, and smoking is a risk factor, not associated with serous tumors.

Unfortunately, it does not have specific signs and symptoms, being associated with an aggressive evolution and a poor prognosis if left untreated. Their results suggest that PD-1 and PD-L1 could be potential biomarkers for targeted treatment in some patients diagnosed with diffuse large B-cell lymphoma. Malignant lymphomas of the head and neck may raise therapeutic difficulties. OIU, Vlad D. In the last five years from 1st of January to 31st of Decemberwe noticed 6 cases of rectal cancer, developed in patients who underwent stoma reversal more than two years before, for different pathologies.

Mucinos tumors are composed of gastrointestinal type cell containing intracytoplasmic mucin and therefore, malignant tumors should always be carefully examined for excluding metastatic tumors with similar morphology 2,5. Endometrioid tumors of the ovary are similar to endometrioid tumors of the endometrium.

A clinical-pathological study of ovarian tumors - one-year center experience

Other rare epithelial tumors include: clear cell tumors, Brenner tumors, mixed serous-mucinous or mixed epithelial-mesenchymal tumors. The group includes: teratomas mature, immature and monodermal or highly specializeddysgerminoma, Yolk-sac tumor, non-gestational chorio-carcinoma, embryonal carcinoma and mixed tumors. In this group, only mature teratomas and monodermal teratoma - benign struma ovarii are benign tumors.

The purpose of this paper is to quantify the in­ci­dence of different histological types of ovarian tumors and to demonstrate the clinical importance of an effective screening program, considering the paucisymptomatic na­ture of this pathology. The incidence of ovarian epithelial tumors varied across age groups, our study group including women aged between 34 and 64 years old. Knowing the age distribution plays an important role in the implementation of screening pro­grams. All cases presented with similar symptomatology: pelvic pain, abdominal distension and ascites.

Sex-cord stromal tumors include neoplasms that contain granulosa cells, theca cells, fibloblasts, Sertoli cells and Leydig cells, which are derived from ovarian­ stroma, that is formed from sex cords under the influences of coelomic and mesonephric epithelium.

This type of tumor has clinical importance because of its potential to elaborate large amounts of estrogens and because it has malignant potential. Pure fibromas are hormonally inactive; Sertoli and Leydig cell tumors are active and have masculinizing or de-fe­mi­nization effects 5,7.

Metastases derived from non-gynecological sites are eleven times more frequent than those derived from female genital organs, the gastrointestinal tract being peritoneal cancer of gynecological origin most common origin 7.

Tumors from the stomach, colon, and breast are the three most common neoplasms that metastasize to the ovary 8. Materials and method We performed a retrospective analysis of ovarian tumor cases registered at the Pathology Department of the Bucharest Emergency University Hospital for a period of one peritoneal cancer of gynecological origin.

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The study included 58 cases of oophorectomy, salpingo-oophorectomy or hysterectomy specimens diagnosed with benign, borderline or malignant tumors of various histologic types. We classified them according to their morphologic features, we analyzed the age distribution for each category, the clinical manifestations, regional spread, lymph nodes status, peritoneal involvement or metastases in available cases; the follow-up was possible in a limited number of cases.

All data was obtained from medical records and from the Statistics Department of University Emergency Hospital in Bucharest. Results and peritoneal cancer of gynecological origin Based on their tumoral behavior, we had Figure 1 : three cases 4. In our study we found a smaller prevalence of benign tumors of only 4.

Figure 1. The distribution of ovarian tumors over a period of one year The most frequent histologic type among all ovarian tumors was represented by high-grade serous carcinoma Mucinous carcinoma accounted for Studies of molecular alteration have suggested that this tumors do actually progress from endometriosis 4, We had one case of poorly differentiated carcinoma of unknown origin.

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All the metastasis cases were large excision specimens and were integrated in the clinico-pathological context. The gynecological origin is usually less frequent than the gastrointestinal origin, which is the first cause of ovarian metastasis 7,8, Rare primary ovarian tumors were represented by: adult granulosa cell tumor Figure 2clear cell carcinoma, mixed serous-mucinous carcinoma, and undifferentiated pleomorphic sarcoma 1. Figure 2. Intraoperative Amacroscopic B and microscopic C aspect of a voluminous left ovarian cyst in a patient of 60 years old; after the histopathological analysis the diagnose was adult granulosa cell tumor - note the micro-follicular pattern The earliest age of a patient with ovarian tumor was 31 years old for the mixed serous-mucinous carcinoma, a younger age than mean age for this type of tumor, but cases of patients within 16 to 79 years had been previously reported 13, Mean age distribution was: 52 years old for benign tumors, with a range of 45 to 67 years old; 51 years old for borderline tumors, with a range of 32 to 73 years old; 60 years old for malignant tumors, with a range of 31 to 83 years old Figure 3.

Mean age peritoneal cancer of gynecological origin in the category of malignant tumors is shown peritoneal cancer of gynecological origin Figure 4.

We found a higher age range for benign tumors, but considering the fact that they were associated with borderline tumors, we found it acceptable 2,4. Figure 3.

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Age range distribution according to the type of tumor Figure 4. Mean age distribution among malignant ovarian tumors We had two cases of tumoral recurrence with multiple metastases of previous high-grade serous carcinoma in patients of 62 and 70 years old, respectively, and one deceased patient of 75 years old, with undifferentiated pleomorphic sarcoma.

They are highly aggressive tumors with poor prognosis, and can develop in younger patients as well. Kurtoglu et al. The most encountered manifestations were: moderate to severe abdominal pain, distention, ascites and anorexia for malignant tumors and mild abdominal distension and menstrual disorders for borderline together with benign tumors.

The symptoms are usually found in large tumors 16, The treatment of ovarian cancer with molecular targeting therapy, platinum and taxane containing chemotherapy and other specific drugs has improved the prognosis over time Currently, the standard primary therapy for advanced disease involves a combination of maximal cytoreductive surgery and chemotherapy with carboplatin plus paclitaxel or with carboplatin alone. Despite initial high response rates, a large proportion of patients relapse, resulting in peritoneal cancer of gynecological origin peritoneal cancer of gynecological origin challenge 19, Because these patients are not curable, the goal of therapy becomes the improvement in both quality and length of life.

Single-agent paclitaxel, topotecan, or pegylated liposomal doxorubicin have demonstrated activity in this patient population and are peritoneal cancer of gynecological origin treatment options 19, Conclusions In our study, primary malignant tumors are the most frequent type of peritoneal cancer of gynecological origin tumors and their age incidence ranges from the third to the eighth decade.

We found higher prevalence rates for high-grade serous carcinomas. The majority of secondary ovarian tumors we studied were of endometrial origin, which may suggest that gynecological primary situs can be considered of greater potential of spreading to the ovaries than previously thought.

Bibliografie 1. Jha R, Karki S. Histological pattern of ovarian tumors and their age distribution. Nepal Med Coll J.

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Robbins and Cotran. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries in Eur J Cancer, ; Sixth Edition. London, Springer Science Business Media, ; Synchronous endometrioid carcinoma of the uterine corpus and ovary.

A case report and review of the literature. Eur J Gynaecol Oncol. Nucci MR, Oliva E.

Gynecologic Pathology. Churchill Livingstone Elsevier; Pathways of metastases from primary organs to the ovaries. Obstet Gynecol Intal,ID Lengyel E. Ovarian cancer development and metastasis. Am J Pathol, ; 3 : — The histologic type and stage distribution of ovarian carcinomas of surface epithelial origin. Int J Gynecol Pathol, ;23 1 Int J Gynecol Pathol, ;30 6 : — Secondary Ovarian Neoplasia.

Utilitatea imunohistochimiei în diagnosticul carcinomului ovarian

A Clinicopathologic study of 35 cases cancer ; Ovarian seromucinous carcinoma: report of a series of a newly categorized and uncommon neoplasm. Am J Surg Pathol, ;39 7 Clinicopathologic study of seromucinous carcinoma of ovary.

Anatomy and Embryology Department University of Medicine and Pharmacy Iuliu Haåieganu, Clinicilor street Cluj Napoca, Romania Received: Accepted: Rezumat Introducere: Carcinomatoza peritoneală reprezintă un stadiu avansat al cancerelor abdominale în general şi a cancerului colorectal în particular. Singurele metode de tratament disponibile la momentul actual pentru această patologie sunt chimioterapia sistemică caracter paliativ şi chirurgia citoreductivă CR asociată cu chimioterapie intraperitoneală hipertermică HIPEC. Material şi metodă: În lucrarea de faţă am analizat prospectiv rezultatele imediate peritoneal cancer of gynecological origin obţinutede către echipa noastră la primii 50 de pacienţi operaţi pentru carcinomatoză peritoneală de diferite origini. În ceea ce priveşte originea histopatologică, 30 de paciente au avut cancer ovarian; 19 pacienţi au avut carcinomatoză cu origine colorectală sau pseudomixom peritoneal de origine apendiculară. Nu a existat mortalitate la 30 de zile.

Undifferentiated pleomorphic sarcoma with focally rhabdomyosarcomatous differentiation of the ovary. Eur J Gynaecol Oncol, ;37 3 Giant ovarian mucinous cystadenoma with borderline areas: a case report. Rom J Morph Embryo, ;55 4 Granulosa cell tumor of the ovary Ginecologia.

Improvement in the prognosis of ovarian cancer in the era before addition of molecular targeting therapy. Jpn J Clin Oncol,; Optimal chemotherapy treatment for women with recurrent ovarian cancer.

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Curr Oncol, ;14 5 A systematic overview of chemotherapy effects in ovarian cancer. Acta Oncol, ;40

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