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1.
J Cancer Res Ther ; 2020 Sep; 16(4): 737-744
Article | IMSEAR | ID: sea-213695

ABSTRACT

Aims: In this study, we investigated the expression of thyroid transcription factor-1 (TTF-1) in lung adenocarcinoma patients' samples and analyzed the association of TTF-1 with clinicopathological parameters, prognosis, and treatment options in patients with lung adenocarcinoma. Subjects and Methods: This retrospective study enrolled 200 patients who were histologically confirmed lung adenocarcinoma with Stage I-IV disease, between 2008 and 2015 years. The cytological archive of these hospitals' Pathology Department was searched. The available slides and the clinical information were reviewed and correlated. All analyses were conducted by SPSS version 15.0 statistical software. Results: Sixty-five (32.5%) of the patients showed TTF-1 negativity and 135 (67.5%) of them showed TTF-1 positivity. The median survival for TTF-1 positive and negative patients was 19.6 and 12.2 months, respectively. We did not find any statistical significance in-between the parameters in terms of the survival data. In TTF-1-negative group, the survival time of epidermal growth factor receptor mutation positive (P = 0.049), cytokeratin 7 (CK7) positive (P = 0.009) patients and those who had received curative radiotherapy (P = 0.028) was significantly better as compared to TTF-1-positive group. We also analyzed the relation between TTF-1 and survival outcome or chemotherapy selection in Stage IV disease. We could not identify any correlation between TTF-1 and survival outcome or treatment selection. Conclusions: This study suggests that TTF-1 is not a favorable prognostic factor in lung adenocarcinoma patients. The prognostic role of CK7 and relationship between TFF-1 expression in lung adenocarcinoma and predictive role of TTF-1 expression for the selection of first-line treatment in Stage IV lung adenocarcinoma should be validated in prospective and randomized studies

2.
Annals of Dermatology ; : 99-103, 2013.
Article in English | WPRIM | ID: wpr-136266

ABSTRACT

Skin metastasis of primary gallbladder tumors is extremely rare with a reported incidence of 0.7~9% and it usually involves the thorax, abdomen, the extremities, neck, head region, and scalp. Cutaneous metastasis may occur synchronously or metatochronously. In the present case, the patient had chronic lymphocytic leukemia, which was being treated with an alkylating agent (chlorambucil) when the patient developed skin metastasis from gallbladder adenocarcinoma during post- cholecystectomy follow-up. Given the fact that secondary malignancies occur in chronic lymphocytic leukemia; this clinical setting warrants attention. We aimed to discuss secondary malignancy in chronic lymphocytic leukemia patients and gallbladder adenocarcinoma with skin metastasis, based on a review of the literature and the presented case.


Subject(s)
Humans , Abdomen , Adenocarcinoma , Cholecystectomy , Extremities , Follow-Up Studies , Gallbladder , Gallbladder Neoplasms , Head , Incidence , Leukemia, Lymphocytic, Chronic, B-Cell , Neck , Neoplasm Metastasis , Scalp , Skin , Thorax
3.
Annals of Dermatology ; : 99-103, 2013.
Article in English | WPRIM | ID: wpr-136263

ABSTRACT

Skin metastasis of primary gallbladder tumors is extremely rare with a reported incidence of 0.7~9% and it usually involves the thorax, abdomen, the extremities, neck, head region, and scalp. Cutaneous metastasis may occur synchronously or metatochronously. In the present case, the patient had chronic lymphocytic leukemia, which was being treated with an alkylating agent (chlorambucil) when the patient developed skin metastasis from gallbladder adenocarcinoma during post- cholecystectomy follow-up. Given the fact that secondary malignancies occur in chronic lymphocytic leukemia; this clinical setting warrants attention. We aimed to discuss secondary malignancy in chronic lymphocytic leukemia patients and gallbladder adenocarcinoma with skin metastasis, based on a review of the literature and the presented case.


Subject(s)
Humans , Abdomen , Adenocarcinoma , Cholecystectomy , Extremities , Follow-Up Studies , Gallbladder , Gallbladder Neoplasms , Head , Incidence , Leukemia, Lymphocytic, Chronic, B-Cell , Neck , Neoplasm Metastasis , Scalp , Skin , Thorax
4.
Saudi Medical Journal. 2006; 27 (9): 1329-1333
in English | IMEMR | ID: emr-80925

ABSTRACT

To determine the association between thymidine phosphorylase [TP] and angiogenesis, and other conventional prognostic markers. We also evaluated interobserver and intraobserver reliability for TP expression in ductal carcinoma, to achieve a more consistent results. Our study included all cases diagnosed in Adnan Menderes University Medical Faculty Hospital, Aydin, Turkey as invasive ductal carcinoma or ductal carcinoma in situ [DCIS] with proven component of [>30%], between January 2003 and February 2005. The total number of the cases was 27 and their median age was 50 years. All sections were stained using monoclonal antibody-TP and examined at x40 magnification. Either nuclear or cytoplasmic staining was accepted as positive. The histoscore [H-score] was calculated for each specimen. The tumor stromal vascularity was assessed by monoclonal anti-CD34; and areas of intense vascularization were determined. Conventional immunohistochemical markers such as c-erb B2, Ki-67, estrogen and progesterone receptors and p53 were also applied to all slides. Three pathologists blindly examined each slide under 10 high-power fields [10 HPF] for 2 times in a 2 months period. There was no significant association between stromal vascularity and TP staining of cancer cells [p=0.1] and no correlation was determined between H-scores for TP staining in ductal carcinoma and DCIS components [p=0.5]. There was no significant correlation noted between stromal and periductal vascularity with the anti-CD34 antibody was used. No significant correlation was identified between the TP H-score and stromal or periductal vascularity


Subject(s)
Humans , Female , Carcinoma, Ductal, Breast/enzymology , Carcinoma, Ductal, Breast/blood supply , Breast Neoplasms/enzymology , Antigens, CD34/metabolism , Microcirculation , Immunohistochemistry , Neoplasm Proteins/metabolism , Neovascularization, Pathologic/enzymology
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