Melanoma, Cutaneous Malignant

  • 文章类型: Case Reports
    背景:恶性黑色素瘤(MM)是最常见和最致命的皮肤癌之一。黑素细胞的恶性转化。它约占全球癌症诊断的1.7%,是美国第五大最常见的癌症。MM几乎可以转移到身体的任何部位,早期检测显著改善预后。病例介绍:我们报告了一名81岁的女性,有恶性黑色素瘤(左小腿原发性病变)和各种合并症的病史。她表现为不明原因的严重贫血。根据她的病史做了CT扫描,揭示了一个圆周,腹下回肠环水平的不对称顶叶增厚。病变提示肿瘤底物。随后的结肠镜检查显示没有转移性病变,但手术证实恶性黑色素瘤回肠转移。患者接受了腹腔镜节段切除术,术后效果良好。切除组织的组织病理学检查证实了恶性黑色素瘤小肠继发性病变的诊断。结论:该病例强调了有MM病史和胃肠道症状模糊的患者考虑转移性黑色素瘤的必要性。通过先进的成像和内窥镜技术进行早期准确的诊断可以显着改善患者的预后。
    Background: Malignant melanoma (MM) is one of the most prevalent and deadliest forms of skin cancer, resulting from the malignant transformation of melanocytes. It accounts for approximately 1.7% of global cancer diagnoses and is the fifth most common cancer in the US. MM can metastasize to almost any part of the body, with early detection significantly improving prognosis. Case presentation: We report the case of an 81-year-old female with a history of malignant melanoma (primary lesion on the left calf) and various comorbidities. She presented with severe anemia of unknown origin. A CT scan was performed due to her medical history, revealing a circumferential, asymmetrical parietal thickening at the level of a hypogastric ileal loop. The lesion suggested a tumoral substrate. Subsequent colonoscopy showed no metastatic lesions, but surgical intervention confirmed a malignant melanoma ileal metastasis. The patient underwent laparoscopic segmental resection with favorable post-surgery outcomes. Histopathological examination of the resected tissue confirmed the diagnosis of small intestine secondary lesions from the malignant melanoma. Conclusion: This case underscores the necessity of considering metastatic melanoma in patients with a history of MM and vague gastrointestinal symptoms. Early and accurate diagnosis through advanced imaging and endoscopic techniques can significantly improve patient outcomes.
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  • 文章类型: Case Reports
    皮肤恶性黑色素瘤(cMM)可以在任何部位发展,但是三分之一的病例主要影响下肢,脚踝和足部病变占所有病例的3-15%。然而,当cMM表现为临床上与糖尿病患者的其他下肢溃疡难以辨别的慢性溃疡时,cMM可能成为临床难题。我们介绍了一个71岁的女性患者,有长期的糖尿病史,高血压,肥胖,慢性肾脏病和心力衰竭患者出现足跟溃疡到我们医院就诊。该病变最初在另一家医院作为神经性糖尿病足溃疡(DFU)进行管理,通过多个局部伤口清创术治疗。然而,溃疡进展为足跟损伤,影响患者的活动能力和生活质量。因此,该患者被转介至我们的糖尿病足专科服务进行进一步治疗。病灶的切除活检显示了cMM。正电子发射断层扫描/计算机断层扫描显示高代谢同侧腹股沟淋巴结病,和右脑转移开始姑息化疗。考虑了免疫疗法,但病人在开始之前就死了.糖尿病患者的非典型足部溃疡需要谨慎的诊断方法,特别是对于对标准疗法没有反应的顽固性皮肤病变。认真管理,在获得组织病理学诊断方面没有不适当的延迟,可能导致黑色素瘤的早期诊断和潜在的更有利的结果。这个案例突出了考虑不典型足部病变的重要性,在一般实践中,除了转诊中心,试图识别令人震惊的特征并采取相应的行动。
    Cutaneous malignant melanoma (cMM) can develop at any site, but one-third of cases primarily affect the lower extremities, with ankle and foot lesions representing 3-15% of all cases. However, cMM may become a clinical conundrum when it presents as chronic ulceration that is clinically indiscernible from other lower extremity ulcers in patients with diabetes. We present the case of a 71-year-old female patient with a longstanding history of diabetes, hypertension, obesity, chronic kidney disease and heart failure who presented to our hospital with a fungating heel ulcer. The lesion was initially managed in another hospital as a neuropathic diabetic foot ulcer (DFU), treated by multiple local wound debridement. However, the ulcer progressed into a fungating heel lesion that interfered with the patient\'s mobility and quality of life. Consequently, the patient was referred to our specialist diabetic foot service for further management. Excisional biopsy of the lesion disclosed a cMM. Positron emission tomography/computed-tomography scanning revealed hypermetabolic ipsilateral inguinal lymphadenopathy, and a right cerebral metastasis for which palliative chemotherapy was initiated. Immunotherapy was considered, but the patient died before it was started. Atypical foot ulcers in patients with diabetes warrant a careful diagnostic approach, especially for recalcitrant cutaneous lesions not responding to standard therapies. Conscientious management, without undue delay in obtaining a histopathological diagnosis, might lead to early diagnosis of melanoma and potentially more favourable outcomes. This case highlights the importance of consideration of atypical foot lesions, in general practice in addition to referral centres, to try to identify alarming features and act accordingly.
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  • 文章类型: Case Reports
    癌症疫苗作为免疫疗法的选择正在取得进展。我们以前已经在皮肤黑色素瘤(CM)患者中证明了用VACCIMEL辅助治疗,四种照射的CM细胞系与BCG和GM-CSF共佐剂的混合物,增加对黑素细胞分化抗原的细胞免疫反应,癌症-睾丸抗原和新抗原,关于基础水平。另一方面,还已知用抗PD-1单克隆抗体(MAb)治疗,作用于预先存在的肿瘤反应性淋巴细胞,在CM患者中诱导临床反应,尽管在一小部分接受治疗的患者中。因此,两种治疗的组合似乎是理想的。在本文中,我们描述了CM患者,即使在接种疫苗后几年也取得了进展,用抗PD-1单克隆抗体治疗。在5/5的此类进展患者中,获得了持续3至65个月的完整响应。其中三名患者保持无病状态,两名复发。其中一名患者在脑转移复发后去世。我们建议VACCIMEL诱导的克隆扩增的反应性淋巴细胞部分保留为记忆细胞,这可能会在肿瘤复发后被召回,并可能促进抗PD-1单克隆抗体的先兆活性。
    Cancer vaccines are gaining ground as immunotherapy options. We have previously demonstrated in cutaneous melanoma (CM) patients that adjuvant treatment with VACCIMEL, a mixture of four irradiated CM cell lines co-adjuvanted with BCG and GM-CSF, increases the cellular immune response to melanocyte differentiation antigens, cancer-testis antigens and neoantigens, with respect to basal levels. On the other hand, it is also known that treatment with anti-PD-1 monoclonal antibodies (MAbs), acting on pre-existing tumor-reactive lymphocytes, induces clinical responses in CM patients, albeit in a fraction of treated patients. A combination of both treatments would appear therefore desirable. In this paper, we describe CM patients who, having progressed even years after vaccination, were treated with anti-PD-1 MAbs. In 5/5 of such progressor patients, complete responses were obtained which lasted between 3 and 65+ months. Three of the patients remain disease-free and two recurred. One of the patients passed away after a recurrence of brain metastases. We suggest that clonally expanded reactive lymphocytes induced by VACCIMEL partially remain as memory cells, which may be recalled after tumor recurrence and may foster ulterior activity of anti-PD-1 MAbs.
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  • 文章类型: Journal Article
    目的:文献中讨论了小儿黑甲的自然史和活检排除黑色素瘤的必要性。我们假设在接受甲癣甲床活检的小儿患者中,恶性指甲病理学的发生率较低。
    方法:我们在2007年至2022年期间,对一家机构的54例儿童患者(年龄<18岁)进行了回顾性图表回顾,这些患者表现为黑甲癣并接受了甲床活检。收集的数据点包括患者人口统计学,病史,体检结果,病理报告,和临床照片。进行单变量和多变量分析以评估与高风险病理结果相关的危险因素。
    结果:黑甲癣发病的平均年龄为5.5岁(SD4.4)。首次活检的平均年龄为7.8岁(SD4.3)。体检时,27例患者至少有四个与黑色素瘤有关的特征(不对称性,边界不规则,颜色异质性,直径>1/3的指甲,不断变化的颜色,不断演变的直径,哈钦森的标志)。最常见的病理诊断是黑素细胞痣(35%),具有良性特征的非典型表皮内黑素细胞增生(AIMP)(24%),甲下扁豆(22%),和AIMP相关功能(17%)。没有原位黑色素瘤或侵袭性恶性黑色素瘤的病例。关于多元回归,与更多相关病理相关的唯一显著危险因素(具有相关特征的AIMP)是进行活检的日历年(系数=-0.34,P=0.016).体检特征与高危病理之间没有关联。12例患者手术再次切除病灶,其中6例是由于AIMP切除不完全,具有相关特征,其中6例是由于复发。
    结论:我们的病例系列没有发现任何由儿童黑甲癣引起的原位黑色素瘤或恶性黑色素瘤病例。具有相关特征的非典型表皮内黑素细胞增生仅与活检的年份相关。这可能反映了对小儿黑甲癣的认识有所提高,尽管其病理特征令人担忧,但通常是良性的。在小儿黑甲癣中进行指甲基质活检的决定应基于患者父母之间的合作讨论,皮肤科医生,和整形外科医生。
    OBJECTIVE: The natural history of pediatric melanonychia and the necessity of biopsy for ruling out melanoma are debated in the literature. We hypothesize that there is a low rate of malignant nail pathology among pediatric patients undergoing nail bed biopsy for melanonychia.
    METHODS: We performed a retrospective chart review of 54 pediatric patients (age <18 years) at a single institution who presented with melanonychia and underwent nail bed biopsy from 2007 to 2022. Data points collected included patient demographics, medical history, physical exam findings, pathology reports, and clinical photos. Univariate and multivariate analyses were performed to assess for risk factors associated with high-risk pathology findings.
    RESULTS: The average age of melanonychia onset was 5.5 years (SD 4.4). The average age of first biopsy was 7.8 years (SD 4.3). On physical exam, 27 patients had at least four features concerning for melanoma (asymmetry, border irregularity, color heterogeneity, diameter > 1/3 of nail, evolving color, evolving diameter, Hutchinson\'s sign). The most common pathology diagnoses were melanocytic nevus (35%), atypical intraepidermal melanocytic proliferation (AIMP) with benign features (24%), subungual lentigo (22%), and AIMP with concerning features (17%). There were no cases of melanoma in situ or invasive malignant melanoma. On multivariate regression, the only significant risk factor associated with more concerning pathology (AIMP with concerning features) was the calendar year in which biopsy was performed (coefficient = -0.34, P = 0.016). There was no association between physical exam features and high-risk pathology. Twelve patients had surgical re-excision of the lesion, 6 of which were due to incomplete excision of AIMP with concerning features and 6 of which were due to recurrence.
    CONCLUSIONS: Our case series did not find any cases of melanoma in situ or malignant melanoma arising from pediatric melanonychia. Atypical intraepidermal melanocytic proliferation with concerning features was associated only with the year in which the biopsy was performed, which may reflect the improved understanding of pediatric melanonychia as often benign despite concerning features on pathology. The decision to perform a nail matrix biopsy in pediatric melanonychia should be based on a collaborative discussion between the patient\'s parents, dermatologist, and plastic surgeon.
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  • 文章类型: Journal Article
    背景:据推测,营养可能会影响皮肤黑色素瘤(CM)的风险;因此,我们旨在评估希腊人群中食物组和个体营养素摄入量与CM的关联。
    方法:在本病例对照研究中,151例经组织学证实的CM,在“Laikon”大学医院肿瘤科(雅典,希腊),和居住在雅典都会区的151名年龄和性别匹配的健康个体,在参与者中招募进行常规健康检查,包括在内。所有参与者都填写了一份包含人体测量的问卷,社会人口统计学,生活方式,和健康相关变量。一个经过验证的,半定量食物频率问卷用于评估发病前12个月内136种食物的平均消费量.使用多变量条件回归模型得出9种食物组和7种常量营养素与CM之间关联的比值比(OR),置信区间为95%(95%CI)。
    结果:发现与CM具有统计学意义的正相关,能量摄入(OR:1.67,95%CI:1.22-2.30)和饱和脂肪酸摄入(OR:2.28,95%CI:1.00-5.28),在调整了对太阳的敏感度之后,抑郁症病史,酒精摄入量。与更高的牛奶和乳制品摄入量的反向关联(OR:0.65,95%CI:0.48-0.88),水果(OR:0.68,95%CI:0.51-0.90),添加脂质(OR:0.65,95%CI:0.47-0.91),还观察到糖和糖浆(OR:0.70,95%CI:0.53-0.93)。
    结论:除了内在风险因素,我们的结果支持CM与多种食物和营养素的关联;如果通过前瞻性研究证实,这些发现可以进一步了解这种致命的癌症。
    BACKGROUND: It has been postulated that nutrition may influence the risk for cutaneous melanoma (CM); therefore, we aimed to assess the associations of food groups and individual nutrient intakes with CM in a Greek population.
    METHODS: In this case-control study, 151 patients with histologically confirmed CM, newly diagnosed and treated in the Oncology Department of the \"Laikon\" University Hospital (Athens, Greece), and 151 age- and sex-matched healthy individuals residing in the Athens metropolitan area, recruited among participants for routine health examinations, were included. All participants completed a questionnaire comprising anthropometric measurements, sociodemographic, lifestyle, and health-related variables. A validated, semiquantitative food frequency questionnaire was used to assess average consumption of 136 food items during the 12 months preceding the onset of disease. Multivariate conditional regression models were used to derive odds ratios (ORs) with 95% confidence intervals (95% CI) regarding the association of nine food groups and seven macronutrients with CM.
    RESULTS: Statistically significant positive associations with CM were found with higher energy intake (OR: 1.67, 95% CI: 1.22-2.30) and intake of saturated fatty acids (OR: 2.28, 95% CI: 1.00-5.28), after adjusting for sun sensitivity, major depression history, and alcohol intake. Inverse associations with higher intake of milk and dairy products (OR: 0.65, 95% CI: 0.48-0.88), fruits (OR: 0.68, 95% CI: 0.51-0.90), added lipids (OR: 0.65, 95% CI: 0.47-0.91), and sugars and syrups (OR: 0.70, 95% CI: 0.53-0.93) were also observed.
    CONCLUSIONS: Beyond intrinsic risk factors, our results support associations of CM with multiple food groups and nutrients; if confirmed by prospective studies, these findings can add further knowledge about this fatal cancer.
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  • 文章类型: Review
    恶性黑色素瘤,一种罕见的儿童皮肤癌,主要影响10岁以上的人。巨大的先天性痣,在大约1%的新生儿中发现,增加了风险。然而,在新生儿期诊断出的先前存在的巨大先天性痣引起的黑色素瘤非常罕见。我们介绍了一个新生儿先天性黑色素瘤的病例,结节生长在婴儿背上现有的痣上。审查了有关管理此类案件的文献。此案例强调了考虑先天性痣恶性转化的重要性及其管理中的挑战。由于报告的病例超过80年,很难提供关于生存和治疗选择的结论性发现.临床医生应报告结果,以开发新生儿黑色素瘤的管理算法。需要进一步的研究来加深对先天性巨大毛痣和相关黑色素瘤患者的病因和治疗的了解。
    Malignant melanoma, a rare skin cancer in children, primarily affects individuals over 10 years old. Giant congenital nevi, found in about 1% of newborns, increases the risk. However, the development of melanoma from a pre-existing giant congenital nevus diagnosed during the neonatal period is exceptionally rare. We present a case of congenital melanoma in a newborn, where nodules grew on an existing nevus on the baby\'s back. Literature on managing such cases was reviewed. This case highlights the importance of considering malignant transformation in congenital nevi and the challenges in their management. Due to limited reported cases over 80 years, conclusive findings on survival and treatment options are difficult to provide. Clinicians should report outcomes to develop a management algorithm for neonatal melanoma. Further studies are needed to enhance understanding of causes and treatment for patients with congenital giant hairy nevi and associated melanoma.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    炎症性肠病(IBD)治疗的基石是免疫调节剂。IBD患者肠道和肠外恶性肿瘤的风险增加。Ustekinumab是一种完全人源化的单克隆抗IL12/23抗体,具有良好的安全性。乳腺恶性肿瘤,结肠,头部和颈部,肾,前列腺,甲状腺,在接受ustekinumab治疗的患者中,有非黑色素瘤皮肤癌的报道.我们报告了一个42岁的克罗恩患者长期接受ustekinumab治疗的病例,患上了消色差恶性黑色素瘤.克罗恩病在15岁时被诊断为上消化道和下消化道受累,最初接受硫唑嘌呤(2mg/kg,持续4年)和英夫利昔单抗(5mg/kg,持续6周)治疗。由于回肠阻塞,患者接受了狭窄成形术,并接受了阿达木单抗(40mg,每隔一周)治疗2年.然后他停止了治疗,一年后接受了右半结肠切除术。阿达木单抗被重新使用(每周40mg),患者保持临床缓解两年。他对阿达木单抗的总暴露时间为四年。Ustekinumab是由于复发而开始的,3年后,头皮瘙痒事件导致诊断为带有BRAFV600E突变的转移性消色差恶性黑色素瘤。他接受靶向治疗,初步反应良好。我们的目的是指出长期免疫抑制的IBD患者发生皮肤恶性肿瘤的风险,以及需要的终身和细致的评估。
    The cornerstone of inflammatory bowel disease (IBD) treatment is immunomodulators. IBD patients are at increased risk of intestinal and extraintestinal malignancy. Ustekinumab is a fully humanized monoclonal anti-IL12/23 antibody with a good safety profile. Malignancies of breast, colon, head and neck, kidney, prostate, thyroid, and non-melanoma skin cancer have been reported among patients who received ustekinumab. We report the case of a 42-year-old Crohn\'s patient on long-term treatment with ustekinumab, who developed achromatic malignant melanoma. Crohn\'s was diagnosed at the age of 15, with upper and lower gastrointestinal involvement and was initially treated with azathioprine (2mg/kg for 4 years) and infliximab (5mg/kg for 6 weeks). Due to ileal obstruction, the patient underwent stricturoplasty and received adalimumab (40mg every other week) for two years. He then discontinued therapy and a year later underwent right hemicolectomy. Adalimumab was reinstituted (40mg every other week) and the patient remained in clinical remission for two years. His overall exposure to adalimumab was four years. Ustekinumab was initiated due to a relapse and after 3 years, an incident of scalp itching led to the diagnosis metastatic achromatic malignant melanoma bearing BRAF V600E mutation. He received targeted therapy with an initial good response. We aim to point out the risk of dermatologic malignancy in IBD patients on long-term immunosuppression and the lifelong and meticulous evaluation that is required.
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  • 文章类型: Case Reports
    肢端淡色黑色素瘤(ALM)是一种传统上在脚底可见的黑色素瘤,手掌,在指甲或脚趾甲下面。它是皮肤黑色素瘤四种组织学亚型中最不常见的黑色素瘤,占所有病例的不到5%。ALM通常在晚期被诊断,并且相对于其他形式的皮肤恶性黑素瘤,在非白种人群中具有更高的发病率。黑色素瘤中最常见的转移部位是皮肤和皮下组织,其次是肺,肝脏,大脑,还有骨头.恶性黑色素瘤骨转移通常发生在已经广泛转移的患者中。我们将本文作为一名84岁的非洲裔美国男性的ALM病变的独特案例研究,最初出现在右第五脚趾足底的底部,然后发现多个骨转移而没有任何其他器官。
    Acral lentiginous melanoma (ALM) is a type of melanoma that is traditionally seen on the soles of the feet, palms of the hand, and under the fingernails or toenails. It is the least frequently diagnosed melanoma among the four histologic subtypes of cutaneous melanoma, accounting for less than 5% of all cases. ALM is frequently diagnosed at late stages and has higher incidences in non-white populations in relation to the other forms of cutaneous malignant melanoma. The most common sites of metastases in melanoma are the skin and subcutaneous tissue followed by lung, liver, brain, and bone. Bone metastases from malignant melanoma usually occur in patients who already have widespread metastases. We present this paper as a unique case study of ALM lesion in an 84-year-old African American male presenting originally in the base of right fifth toe plantar aspect then found multiple bone metastases without any other organ involved.
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  • 文章类型: Case Reports
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