Skin metastases

皮肤转移
  • 文章类型: Case Reports
    卵巢癌的皮肤转移很少见,预后通常较差。我们报告了一例62岁女性复发性低度浆液性卵巢癌,出现肺的人,大脑,和多个皮肤(鼻和前胸壁)转移约6个月后的初步诊断。在这种情况下,由RAD50杂合突变和先前的贝伐单抗治疗引起的Nijmegen断裂综合征携带者状态可能是皮肤转移的诱发因素。患者接受了局部放疗(鼻部皮肤和脑部,30Gy/6f/1.2W)和三个疗程的白蛋白结合型紫杉醇和卡铂化疗,导致皮肤转移的急剧缓解。不幸的是,治疗中断导致肿瘤快速进展,其次是死亡。这个病例代表了卵巢癌皮肤转移的一个有趣的例子,具有罕见的临床表现,独特的基因突变,对治疗的合理反应。放化疗可能是卵巢癌皮肤转移的合适选择。然而,我们仍然希望在将来收集和审查更多病例后找出最佳治疗策略。
    Cutaneous metastases of ovarian cancer are rare and often have poor prognosis. We report a case of a 62-year-old woman with recurrent low-grade serous ovarian cancer, who presented with lung, brain, and multiple skin (nasal and anterior chest wall) metastases approximately six months after the initial diagnosis. In this case, Nijmegen breakage syndrome carrier status caused by RAD50 heterozygous mutation and previous bevacizumab therapy could be the predisposing factor for cutaneous metastases. The patient was treated with local radiotherapy (nasal skin and brain, 30Gy/6f/1.2W) and three courses of chemotherapy with albumin-bound paclitaxel and carboplatin, resulting in drastic remission of the cutaneous metastases. Unfortunately, treatment interruption resulted in rapid tumor progression, followed by death. This case represents an interesting example of cutaneous metastasis of ovarian cancer with rare clinical manifestations, unique genetic mutations, and reasonable response to treatment. Chemoradiotherapy might be an appropriate option for cutaneous metastases of ovarian cancer. Nevertheless, we still hope to find out the best treatment strategy after collecting and reviewing more cases in the future.
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  • 文章类型: Case Reports
    子宫内膜癌的皮肤转移很少见。我们报告了一例54岁的女性,她从子宫内膜癌中发展为皮肤转移,并回顾相关文献,以深入了解这种罕见和严重的情况。
    北京大学人民医院患者的临床病理资料和治疗,是从她的医疗记录中找到的.通过PubMed/MEDLINE进行了关于这种异常疾病进展的系统文献检索。
    一名诊断为IB期子宫内膜样癌的绝经后患者迅速发展为皮肤转移。术后10个月,患者出现多个淋巴结转移,22个月后,两个乳房均出现皮肤转移。然后她接受了化疗,免疫疗法和激素疗法。皮损暂时缓解,但迅速恶化。最终,她在皮肤病变出现后7个月内死亡。
    子宫内膜癌的皮肤转移通常是无法治愈的,并且预后有限。
    Cutaneous metastases of endometrial carcinoma are rare. We report a case of a 54-year-old woman who developed cutaneous metastases from an endometrial carcinoma, and review the related literature to offer insight into this rare and serious condition.
    The clinical and pathological data and therapy delivered to a patient from Peking University People\'s Hospital, were retrieved from her medical records. A systematic literature search regarding this unusual disease progression was conducted through PubMed/MEDLINE.
    A postmenopausal patient diagnosed with stage IB endometrioid carcinoma rapidly developed cutaneous metastases. 10 months postoperatively, the patient developed multiple lymph node metastases, and 22 months later, cutaneous metastases appeared on both breasts. She was then treated with chemotherapy, immunotherapy and hormone therapy. The skin lesions eased temporarily but deteriorated quickly. Ultimately, she died in 7 months subsequent to the appearance of cutaneous lesions.
    Cutaneous metastases from endometrial carcinoma have usually been incurable and associated with a limited prognosis.
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  • 文章类型: Journal Article
    小丑鼻样病变是指在鼻尖上出现带红色或皮肤颜色的凸起或鼻球尖的表现。越来越多的临床病例表明,小丑鼻样病变也可能是某些遗传综合征的指征,不仅仅是最初提出的转移性内脏肿瘤的表现。然而,由转移性恶性肿瘤指示的小丑鼻样病变的临床特征,缺乏涉及鼻尖的遗传性癌症易感性综合征或原发性疾病。在这项研究中,收集并回顾了我们临床实践和已发表文献中的小丑鼻样病变患者。我们发现,由包括肺癌在内的转移性恶性肿瘤引起的小丑鼻样病变通常是孤立的,并且在男性(24/31)老年个体(平均年龄62.3,40-78岁)中更为常见。此外,它们通常出现很短的时间,容易被误诊为原发性鼻部疾病,导致预后不良(所有有数据的患者均在4个月内死亡)。与遗传性癌症易感性综合征相关的小丑鼻样病变通常在年轻时(平均年龄15.3岁)发展,女性偏好(9/10)。它们伴随着多系统的参与,包括低头发量,发育迟缓,癌症易感性或神经系统疾病。他们表现出缓慢的发展和经常积极的家族史(6/10)。这两种小丑鼻样病变往往无症状,这延迟了潜在恶性肿瘤或综合征的诊断和治疗。简而言之,小丑鼻子样病变的术语被低估了,并且应该更新。小丑鼻样病变可以作为至少三类临床问题的指标:转移性内脏肿瘤,遗传综合征,和涉及鼻尖的原发疾病。提高对更新的小丑鼻样病变的临床特征的认识可以提醒医生注意这些潜在的恶性肿瘤或综合征,使早期检测相关的医疗问题,并允许对家庭成员进行遗传咨询。
    Clown nose-like lesion refers to the manifestation of a reddish or skin-colored bulge on the tip of the nose or the manifestation of bulbous tip of the nose. More and more clinical cases show that clown nose-like lesion can also be the indication of some genetic syndromes, not just the manifestation of metastatic visceral tumor as it initially proposed. However, the clinical features of clown nose-like lesion indicated by metastatic malignancies, genetic cancer predisposition syndromes or primary diseases involving the nasal tip are lacking. In this study, patients with clown nose-like lesion in our clinical practices and from published literatures were collected and reviewed. We found that clown nose-like lesions caused by metastatic malignancies including lung cancer are often solitary and more common in male (24/31) older individuals (average age 62.3, ranging 40-78 years old). In addition, they usually appear for a short time, and are prone to be misdiagnosed as primary nasal diseases, leading to a poor prognosis (all patients with data available died within 4 months). Clown nose-like lesions associated with genetic cancer predisposition syndromes usually develop at a young age (mean age 15.3) with female preference (9/10). They are accompanied by multiple-systemic involvements, including low hair volume, developmental delay, cancer predisposition or neurological diseases. They show slow development and often positive family history (6/10). These two kinds of clown nose-like lesions are often asymptomatic, which delays the diagnosis and treatment of underlying malignancies or syndromes. In brief, the term of clown nose-like lesion is underrecognized, and should be updated. Clown nose-like lesions can serve as indicators to at least three categories of clinical issues: metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip. Increased awareness of clinical features of updated clown nose-like lesions can alert physicians to these underlying malignancies or syndromes, render earlier detection of associated medical issues, and allow for genetic counseling of family members.
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