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Journal of Cancer Epidemiology | 2011

Cancers in Togo from 1984 to 2008: Epidemiological and Pathological Aspects of 5251 Cases

Koffi Amegbor; Tchin Darré; Koffi Didier Ayéna; Essohana Padaro; Kodjo Tengue; Anani Abalo; Gado Napo-Koura

Objective. To describe the epidemiological and histological aspects of cancers in Togo. Materials and Methods. We made a retrospective review of the epidemiological and pathological features of cancers observed from 1984 to 2008 at the laboratory of pathology of CHU-TOKOIN in Lomé, Togo. Results. During our study period, we found 5251 cases of cancers with an annual average frequency of 210 cases. The sex ratio, male/female, was 0.9 and the average age of occurring was 45.3 years. This average age was 46.9 years for men and 43.8 years for women. The most frequent cancers for men were prostate cancer (12.9%), nonmelanoma skin cancer (10.4%), and gastric cancer (10.3%). For women it was breast cancer (27.1%), cervix cancer (11.2%) and non-Hodgkin lymphoma (6.3%). Histologically, it was carcinomas in 68.1% of the cases, sarcomas in 11% of the cases and non-Hodgkin lymphomas in 12.6% of the cases. Children cancers were primarily Burkitt lymphoma (27.9% of cases) and retinoblastoma (8.5% of cases). Conclusion. This study shows that cancers are frequent in Togo and emphasizes on the necessity of having a cancer register for the prevention and the control of this disease in Togo.


Annales De Dermatologie Et De Venereologie | 2011

Cas cliniqueLeucodermie en gouttes précoce au cours de la maladie de Darier chez un sujet à peau noireEarly guttate leukoderma in Darier's disease in a patient with black skin

A. Mouhari-Toure; K. Kombaté; B. Saka; Koffi Amegbor; Tchin Darré; S. Akakpo; K. Tchangaï-Walla; P. Pitché

BACKGROUND The clinical manifestations of Dariers disease are polymorphic and diverse. Guttate leukoderma has been described in around twenty patients with genetically pigmented skin. We report a case of widespread guttate leukoderma several years before the classic signs of Dariers disease in a patient with black skin. CASE REPORT A 19-year-old woman consulted for characteristic signs of Dariers disease evolving for the previous four years. Examination revealed perifollicular, non-confluent hypopigmented macules and papules in small drop size (1-5mm in diameter) scattered on the trunk, limbs and the jaw and chin. These hypopigmented lesions had been present since the age of six years. Histology of the keratotic papules confirmed the diagnosis of Dariers disease. Histological inspection of a hypopigmented lesion showed hyperkeratosis, acantholysis and a considerable reduction of epidermal melanin pigment. DISCUSSION Our observation suggests that a guttate leukoderma could be an early sign, readily accessible to dermatologists, in the diagnosis of Dariers disease in black-skinned patients.


Annales De Dermatologie Et De Venereologie | 2011

Leucodermie en gouttes précoce au cours de la maladie de Darier chez un sujet à peau noire

A. Mouhari-Toure; K. Kombaté; B. Saka; Koffi Amegbor; Tchin Darré; S. Akakpo; K. Tchangaï-Walla; P. Pitché

BACKGROUND The clinical manifestations of Dariers disease are polymorphic and diverse. Guttate leukoderma has been described in around twenty patients with genetically pigmented skin. We report a case of widespread guttate leukoderma several years before the classic signs of Dariers disease in a patient with black skin. CASE REPORT A 19-year-old woman consulted for characteristic signs of Dariers disease evolving for the previous four years. Examination revealed perifollicular, non-confluent hypopigmented macules and papules in small drop size (1-5mm in diameter) scattered on the trunk, limbs and the jaw and chin. These hypopigmented lesions had been present since the age of six years. Histology of the keratotic papules confirmed the diagnosis of Dariers disease. Histological inspection of a hypopigmented lesion showed hyperkeratosis, acantholysis and a considerable reduction of epidermal melanin pigment. DISCUSSION Our observation suggests that a guttate leukoderma could be an early sign, readily accessible to dermatologists, in the diagnosis of Dariers disease in black-skinned patients.


Asian Pacific Journal of Cancer Prevention | 2015

Descriptive Epidemiology of Thyroid Cancers in Togo.

Tchin Darré; bathokedeou amana; Essobozou Pegbessou; Haréfétéguéna Bissa; Koffi Amegbor; essohanam boko; Eyawelohn Kpemessi; Gado Napo-Koura

BACKGROUND The purpose of this study was to provide epidemiological and histological data of thyroid cancers in Togo. MATERIALS AND METHODS This was a retrospective cross-sectional study of cases of thyroid cancers diagnosed from 2000 to 2014 (15 years) at the pathology laboratory of the Sylvanus Olympio Teaching Hospital of Lome. All cases of review of a thyroid sample (biopsies, surgical specimens) were collected from the data records of that laboratory. RESULTS Thyroid cancers represented 1.1% (7930 cases) of all cancers registered during the study period. Mean age was 45.4±0.3 years and the proportion of females was 78.3%. We identified 92.4% carcinomas and 7.6% lymphomas. Carcinomas were well differentiated in 80 cases and were dominated by the papillary type (47 cases). Metastasis was observed in 13% of patients. The pTNM classification evaluated in 18 cases showed a predominance of grade I (13 cases). Lymphomas were dominated by lymphoma diffuse large B-cell (5 cases). CONCLUSIONS This study is the first global standard for thyroid cancer pathology in Togo. The high frequency of follicular form suggests an unrecognized iodine deficiency. The improvement of the technical platform of the LAP (immunohistochemistry) will increase the diagnosis of rare forms of thyroid cancer.


Tropical Doctor | 2018

Tuberculosis of the thyroid in Togo: a clinicopathologic study of 11 presumed cases

Tchin Darré; bathokedeou amana; Essobozou Pegbessou; Foma Winga; Dolou Warou; Gado Napo-Koura

Tuberculosis (TB) remains a real public health concern in Africa; thyroid localisation of the disease is a very rare form of extrapulmonary TB. We conducted a descriptive and cross-sectional study on all histologically proved cases of thyroid TB diagnosed in Togo over the last 20 years. Eleven cases of TB of the thyroid were identified, of which nine were in women, with an average age of 29.4 ± 0.2 years. The clinical signs were the presence of a nodule in seven, an abscess in three and a swelling with cutaneous fistulisation in one. Thyroid involvement alone was found in four, associated with pleuropulmonary TB in six and mammary TB in one. Human immunodeficiency virus (HIV) co-infection was present in six. All histopathology results showed inflammatory granulomata with caseous necrosis. The clinical features are often misleading and pose a real diagnostic problem, especially with differentials of simple abscess and cancer.


Journal of Gastrointestinal Cancer | 2018

Primary Angiosarcoma Pancreas: a Case Report of an Exceptional Localization

Tchin Darré; Mazamaesso Tchaou; Boyodi Tchangaï; Fousseni Alassani; Sassil Dare; Gado Napo-Koura

Pancreas sarcomas are very rare and represent less than 1% of all pancreas cancers [1]. Angiosarcoma is uncommon and has defavorable prognosis [1, 2]. The diagnosis of angiosarcoma is based on histological analysis and differentiated from aciae hemangiopericytoma and Kaposi’s sarcoma [3].We reported a case of primary non-metastatic pancreas angiosarcoma in a 41-year-old man in Togo, confirmed by immunohistochemistry. We described epidemiological, morphological, and immunohistochemical aspects of primary pancreas angiosarcoma.


Urology case reports | 2017

Papillary Renal Cell Carcinoma Revealed by Renal Traumatism: A Case Report in Lomé

Tchilabalo Matchonna Kpatcha; Kodjo Tengue; Gnimdou Botcho; Tchin Darré; Kossi Akomola Sabi; Komi Hola Sikpa; Essomendedou Léloua; Edoé Viyomé Sewa; Obube Amégayibor; Tsipa Anoukoum; Koffi Amegbor; Ekoué David Dosseh

This study is a report on a case of papillary carcinoma of the kidney revealed by an abdominal contusion. The results of radiological investigations were discordant with the low intensity of the shock. The treatment consisted of radical nephrectomy because of the suspicion of a pre-existing malignancy. Histological analysis revealed a papillary carcinoma pT3N0M0. We focus on the need for performing diagnostic tests in order to avoid missing a pre-existing anomaly to the kidney trauma.


Pathology & Oncology Research | 2017

Association of Schistosomiasis with Cervical Cancer in Togo: the Consequence of this Association

Tchin Darré; Abdoul-Samadou Aboubakari; Bingo K. N’Bortche; Akila Bassowa; Gado Napo-Koura

Objective of the study was to determine the association of cervical cancer association and schistosomiasis infection. We conducted a retrospective and descriptive study of cases of cervical cancer and identified cases associated with schistosomiasis. A total of 1027 cases of cervical cancer were collected, and 19 cases revealed an association with schistosomiasis. This association was mainly related to squamous carcinoma with 18/19 cases. All patients were from rural areas. Of the 19 cases of association, 17 cases showed signs of HPV infection. Our data show a high degree of HPV infection that causes cervical cancer and not schistosomiasis.


Molecular and Clinical Oncology | 2017

Breast cancer cases of female patients under 35 years of age in Togo: A series of 158 cases

Tchin Darré; Mazamaesso Tchaou; Koué Folligan; Abdoulatif Amadou; Bidamin N'Timon; Lantam Sonhaye; Abdoul‑Samadou Aboubakari; Koffi Amegbor; Koffi Akpadza; Gado Napo Koura

Breast cancer in young female patients represents a public health problem in developing countries. The objectives of the study were to study the epidemiological and histological characteristics of breast cancer in female patients under 35 years of age. This was a retrospective analytical study of a series of 158 cases of breast cancer in female patients under 35 years of age, conducted at the University Teaching Hospital of Lomé between 2000 and 2015. A total of 158 cases were collected, representing 36.2% (436) of all breast cancer cases. The average age of the patients was 30.9 years (range, 16-35 years). A family history of breast cancer at the 1st or 2nd degree was identified in 13.9% of cases. Genetic mutation studies were carried out for 7 patients, 5 of which revealed mutations (4 BRCA1 and 1 BRCA2). According to the locus, the cancer was located preferentially in the left breast in 88 cases (55.7%). Malignant mammary lesions were epithelial tumors (n=144 cases, 91.1%), infiltrating (n=125 cases, 79.1%) and non-infiltrating (n=19 cases, 12.0%). The other histological groups consisted of 8 cases of sarcomas (5 cases of angiosarcoma, 2 cases of fibrosarcoma and 1 case of Kaposis sarcoma), 5 cases of lymphomas and one case of melanoma. Not otherwise specified infiltrating ductal carcinomas were SBR II and III in 43.2 and 35.2% of cases, respectively. The tumors classified as T4 were the most frequent (30.4%). Regarding the lymph node status, lymph node metastasis was noted in 22.8% of cases. Studies of hormone receptors were carried out in 23 patients and were positive for 11 patients: Estrogen receptor (ER)+plus progesterone receptor (PR)+(7 patients), ER+PR-(4 patients). Of the aforementioned 8 cases of sarcoma, 5 were angiosarcoma. The lymphomas were predominantly Burkitts type for 4 cases. Mammary ultrasonography was performed in 45.6% of the patients and 54.4% underwent the combined ultrasonography and mammography. Ultrasound identified one or more sign of malignancy in 67 patients (42.4%), and combined ultrasonography and mammography classified 51.9% of lesions in BIRADS 4 and 5. The incidence of breast cancer in young Togolese patients is high. It is a disease distinguished by a delay in diagnosis, which contributes to the high number of cases that initially diagnosed at an advanced stage, particularly the high histo-prognosis grades of infiltrating ductal carcinoma. These results indicate a genetic origin; therefore, a thorough investigation into genetic mutations should be carried. In addition, further collaborative studies are required to verify these results.


Journal of pathogens | 2017

Histoplasmosis by Histoplasma capsulatum var. duboisii Observed at the Laboratory of Pathological Anatomy of Lomé in Togo

Tchin Darré; Bayaki Saka; Abas Mouhari-Toure; Améyo Monique Dorkenoo; Koffi Amegbor; Vincent Palokinam Pitche; Gado Napo-Koura

Our study aimed to describe the epidemiological, clinical, and diagnostic aspects of African histoplasmosis in Togo through a descriptive and cross-sectional study on histological diagnosed African histoplasmosis in Pathology Department of Lomé from 2002 to 2016 (15 years). A total of 17 cases of African histoplasmosis were diagnosed. The sex ratio (M/F) was 1.8. The annual incidence was 1.1 cases. The mean age of the patients was 27.2 ± 0.4 years. All our patients were of social categories with a low socioeconomic level. HIV infection was known in 3 patients and one patient contracted tuberculosis. The clinical manifestations were cutaneous in 7 cases, cutaneous and mucous in 3 cases, cutaneous and lymph node in 3 cases, cutaneous and bone in 2 cases, and disseminated in 2 cases. The samples examined consisted of 14 cutaneous biopsies measuring 2-3 cm and 3 ganglionic biopsies each measuring 4 cm of major axis. Histologically, all cases were of chronic form made of granulomatous reaction with ovoid yeasts measuring between 1 and 2 microns. Despite the low frequency of this disease in our country, it should be kept constantly in mind before any granulomatous lesions, especially in the context of the HIV pandemic.

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