ADRENOCORTICAL CARCINOMA IN A 2 YEAR OLD CHILD, A RARE ENTITY

A. Agarwal, S. Bharti
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Abstract

Adrenocortical carcinomas are a rare type of malignancy, particularly in children. There is no such gender predilection with both male and female preponderance in different studies. Early diagnosis and treatment are necessary for better prognosis as well as its differentiation from entities like adrenocortical adenoma and phaeochromocytoma. Here, we describe a case of adrenocortical cancer in a 2-year-old child who had virilistic symptoms, hirsutism and weight gain. Her tanner stage was II. On histomorphology Weiss score was 8 and Wieneke AFIP score was 6. Patient received timely chemotherapy after surgery
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2岁儿童肾上腺皮质癌,罕见病例
肾上腺皮质癌是一种罕见的恶性肿瘤,尤其是在儿童中。在不同的研究中并没有这样的性别偏好,男性和女性都占优势。早期诊断和治疗对于改善预后以及与肾上腺皮质腺瘤和嗜铬细胞瘤等实体进行鉴别是必要的。在这里,我们描述一个2岁儿童肾上腺皮质癌的病例,他有男性化的症状,多毛和体重增加。她的晒黑阶段是II。组织形态学上,Weiss评分为8分,Wieneke AFIP评分为6分。术后患者及时接受化疗
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DELTA-9 TETRAHYDROCANNABINOID AND GEMSITABIN COMBINATION ON NON-SMALL CELL (SQUAMOUS CELL, SK-MES-1) LUNG CANCER CELL LINE CESAREAN SECTION INDICATIONS USING MODIFIED ROBSON’S CRITERIA TOTAL LUNG COLLAPSE TREATED WITH EFFECTIVE PHYSIOTHERAPY AND PHARMACOTHERAPY ADRENOCORTICAL CARCINOMA IN A 2 YEAR OLD CHILD, A RARE ENTITY EFFECT AND IMPLICATION OF BRONCHOSCOPIC BALLOON DILATATION IN A CASE OF TOTAL LUNG COLLAPSE
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