ADENOSQUAMOUS LUNG CARCINOMA COMPLICATED WITH MARANTIC ENDOCARDITIS AND CHRONIC DISSEMINATED INTRAVASCULAR COAGULATION

Andreea-Daniela Scînteie, R. Vasile, C. Diaconu
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Abstract

Background: Adenosquamous lung carcinoma is a relatively rare subtype of non-small-cell lung cancer that contains both adenocarcinoma (ADC) and squamous cell carcinoma (SCC) components. It is difficult to reach a proper diagnosis before surgery, with the histopathological examination of the resected specimen being the method of choice. A supplementary immunohistochemistry examination of the sample is needed. In order to initiate targeted treatment, molecular testing is mandatory. Case presentation: A 47-year-old female, smoker (15 packs-year), without pathological personal history, presented for fatigue and moderate bilateral leg edema for about 3 months. The blood tests showed severe microcytic, hypochromic anemia and chronic disseminated intravascular coagulation. Computed tomography (CT) scan revealed a tumor in the right basal pleura with secondary pleural effusion, multiple lymphadenopathies, disseminated in the mediastinum, abdominal and pelvic cavity. Two other tumors were noticed, one in the right breast (7 mm) and the other in the vesicouterine pouch (7/10 mm). Prior to lung biopsy, a transthoracic and then transesophageal echocardiography were performed, highlighting the presence of a band on the aortic valve, suggesting marantic endocarditis. Tumor markers were also elevated. In evolution, the patient became bradypsychic, with head CT showing a brain metastasis in the left high-parietal region. Immunohistochemistry examination of the biopsy sample suggested a adenosquamous lung carcinoma. Conclusion: We reported the diagnostic path of a rare subtype of lung cancer in a young female without known comorbidities, with an atypical presentation - multiple extrapulmonary non-metastatic manifestations: metabolic etiology - weight loss, fatigue; vascular and hematological etiology – marantic endocarditis (a very rare complication), severe microcytic, hypochromic anemia and chronic disseminated intravascular coagulation; neurological etiology – peripheral sensorimotor neuropathy of the right arm. A tissue biopsy was performed from the most accessible region – 1/3 inferior right thorax, posterior axillary line. The particularity of the adenosquamous lung carcinoma in this case lies in multiple metastases in less common sites (breast, vesicouterine pouch and probably kidney).
肺腺鳞癌并发血管性心内膜炎和慢性弥散性血管内凝血
背景:腺鳞肺癌是一种相对罕见的非小细胞肺癌亚型,包含腺癌(ADC)和鳞状细胞癌(SCC)成分。手术前很难做出正确的诊断,切除标本的组织病理学检查是选择的方法。需要对样本进行补充免疫组织化学检查。为了启动靶向治疗,分子检测是必须的。病例介绍:47岁女性,吸烟(15包/年),无个人病理史,因疲劳、双侧腿部中度水肿约3个月。血液检查显示严重的小细胞性、低色性贫血和慢性弥散性血管内凝血。CT扫描显示右侧基底胸膜肿瘤伴继发性胸膜积液,多发淋巴结病变,播散于纵隔、腹腔及盆腔。另外两个肿瘤,一个在右乳(7毫米),另一个在膀胱外袋(7/10毫米)。在肺活检前,行经胸和经食管超声心动图检查,发现主动脉瓣上有带状带,提示血管性心内膜炎。肿瘤标志物也升高。在进化过程中,患者变得精神迟钝,头部CT显示左侧高顶叶脑转移。活检标本免疫组化检查提示肺腺鳞癌。结论:我们报告了一名年轻女性肺癌罕见亚型的诊断路径,无已知合并症,非典型表现-多发性肺外非转移性表现:代谢病因-体重减轻,疲劳;血管性和血液学病因-血管性心内膜炎(一种非常罕见的并发症),严重的小细胞性、低色度贫血和慢性弥散性血管内凝血;神经病因学-右臂外周感觉运动神经病。在最容易到达的区域-右胸下1/3,腋窝后线处进行组织活检。本例腺鳞肺癌的特殊性在于多发转移部位(乳腺、膀胱外囊,可能还有肾脏)。
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