绒毛膜癌的肺转移:“化疗前后”

S. Singla, Sunesh Kumar, K. Roy, J. Sharma, Neeta Singh
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引用次数: 1

摘要

病例总结:这是一个26岁的女性,在她提出一年不规则阴道出血和五个月咯血的主诉后,被诊断为绒毛膜癌。这是在一年前的一次流产后发生的,那次流产是在其他地方进行的扩张和刮宫。以前有过一次足月分娩和两次流产的历史。刮除的组织病理学显示坏死背景中有少量非典型细胞伴轻度炎症细胞浸润。当她来到我们研究所时,我们做了一个完整的转移性检查,包括全血细胞计数、肝功能检查和血清β-HCG水平。基线血液检查在正常范围内,入院时血清β-HCG水平为6,37,000 IU/ml。图1:化疗前胸部x线片示“炮弹状”肺转移。胸部x线检查显示肺转移(图1),表现为“炮弹转移”。胸部增强CT (CECT)证实肺转移。腹部CECT显示子宫体积庞大,面积为4x3x3.5 cm,双肾多发梗死伴单纯性囊肿。CECT头部正常。根据FIGO风险评分系统,患者评分为12分(妊娠滋养细胞瘤高风险)。患者于第1天和第2天给予EMA-CO化疗,即依托泊苷、甲氨蝶呤和放线菌素;第8天使用环磷酰胺和长春新碱。经过4个周期的EMA-CO治疗后,她的β-HCG水平降至2467.49 IU/ml,胸部x线片也显示转移灶的明显消退(图2)。图2:化疗后病变的胸部x线片显示绒毛膜癌的肺转移:“化疗前后”3个中的2个背景肺转移是常见的,最常见于系统性静脉引流丰富的肿瘤。此类转移的例子包括肾癌、骨肉瘤、绒毛膜癌、黑色素瘤、睾丸畸胎瘤和甲状腺癌。胸部x线通常是诊断转移的第一影像学方式。重要的是要认识到这些病变,因为它改变了疾病的阶段和治疗过程。在绒毛膜癌中,通常60%的患者在发病时有肺转移,在70-100%的病例中,尸检时发现肺病变。肺转移的存在是一个不良的预后因素,表明疾病播散。在绒毛膜癌中,肺转移的存在将病变升级为III期疾病,需要联合多药化疗- emaco。然而,对化疗敏感的肿瘤,如绒毛膜癌和睾丸畸胎瘤,预后较好。肿瘤可表现为肺结节,如图1所示。肺结节是肺部继发性肿瘤疾病最常见的表现。它们通常来源于肿瘤栓塞,肿瘤栓塞是由肿瘤毛细血管的侵犯引起的。肿瘤栓子经全身静脉和肺动脉排出,随后停留在小肺动脉或小动脉中,并延伸到邻近的肺组织。化疗可改变这些病变的外观(图2)。完全解决是罕见的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary metastasis in Chorio-carcinoma: “Before and After Chemotherapy”
CASE SUMMARY This is a case of a 26-yr old lady who was diagnosed to have chorio-carcinoma, after she presented with complaints of irregular vaginal bleeding for one year and hemoptysis for five months. This was following a missed abortion one year back for which dilatation and curettage was done elsewhere. There was a history of one previous full term child birth and two abortions previously. Histopathology of the curettage had revealed few atypical cells in necrotic background with mild inflammatory cell infiltration. When she presented to our institute, a complete metastatic work-up including complete blood counts, liver function tests and serum β-HCG level was done. Baseline blood investigations were within normal limits and serum β-HCG levels at admission was 6, 37,000 IU/ml. Figure 1 Figure 1: Chest X-Ray showing “cannon-ball” pulmonary metastasis before chemotherapy. Chest X-Ray was done which showed evidence of pulmonary metastasis (Figure 1) in the form of “cannon-ball metastasis”. Contrast enhanced CT (CECT) chest confirmed the pulmonary metastasis. CECT abdomen had revealed a bulky uterus with 4x3x3.5 cm intense heterogeneously enhancing area and multiple infarcts in both kidneys with presence of a simple cyst. CECT head was normal. According to FIGO risk scoring system, her score was 12 (high risk Gestational trophoblastic neoplasia). Patient was administered EMA-CO chemotherapy i.e. Etoposide, Methotrexate and Actinomycin on Day 1 and 2; Cyclophosphamide and Vincristine on day 8. After 4 cycles of EMA-CO, her β-HCG levels fell down to 2467.49 IU/ml and chest X-Ray too showed significant resolution of metastatic lesions (Figure 2). Figure 2 Figure 2: Chest X-Ray showing post chemotherapy lesion Pulmonary metastasis in Chorio-carcinoma: “Before and After Chemotherapy” 2 of 3 BACKGROUND Pulmonary metastases are common and most frequently occur with tumors that have rich systemic venous drainage. Examples of such metastases include renal cancers, bone sarcomas, chorio-carcinomas, melanomas, testicular teratomas, and thyroid carcinomas. Chest X-Ray is usually the first imaging modality in which the metastases are diagnosed. It is important to recognize these lesions, as it changes the stage of disease and treatment course. In chorio-carcinoma, usually 60% of patients have pulmonary metastasis at presentation, and in 70-100% cases, the pulmonary lesion is detected at autopsy. The presence of pulmonary metastases is a bad prognostic factor that indicates disseminated disease. In chorio-carcinoma, presence of pulmonary metastasis upgrades the lesion to stage III disease and asks for combination multidrug chemotherapy-EMACO. However, chemo-sensitive tumors, such as chorio-carcinoma and testicular teratoma, have a better prognosis. Tumor may manifest in lungs as pulmonary nodules as in Figure 1. Pulmonary nodules are the most common manifestation of secondary neoplastic disease in the lungs. They are usually derived from tumor emboli that arise from invasion of tumor capillaries. The tumor emboli drain via the systemic veins and pulmonary arteries, subsequently lodging in the small pulmonary arteries or arterioles and extending into adjacent lung tissue. Chemotherapy may change appearance of these lesions (Figure 2). Complete resolution is rare.
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