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Nevoid basal cell carcinoma syndrome (Gorlin syndrome)

机译:避免基底细胞癌综合征(高林综合征)

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摘要

Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms.The estimated prevalence varies from 1/57,000 to 1/256,000, with a male-to-female ratio of 1:1.Main clinical manifestations include multiple basal cell carcinomas (BCCs), odontogenic keratocysts of the jaws, hyperkeratosis of palms and soles, skeletal abnormalities, intracranial ectopic calcifications, and facial dysmorphism (macrocephaly, cleft lip/palate and severe eye anomalies). Intellectual deficit is present in up to 5% of cases. BCCs (varying clinically from flesh-colored papules to ulcerating plaques and in diameter from 1 to 10 mm) are most commonly located on the face, back and chest. The number of BBCs varies from a few to several thousand. Recurrent jaw cysts occur in 90% of patients. Skeletal abnormalities (affecting the shape of the ribs, vertebral column bones, and the skull) are frequent. Ocular, genitourinary and cardiovascular disorders may occur. About 5–10% of NBCCS patients develop the brain malignancy medulloblastoma, which may be a potential cause of early death.NBCCS is caused by mutations in the PTCH1 gene and is transmitted as an autosomal dominant trait with complete penetrance and variable expressivity.Clinical diagnosis relies on specific criteria. Gene mutation analysis confirms the diagnosis. Genetic counseling is mandatory. Antenatal diagnosis is feasible by means of ultrasound scans and analysis of DNA extracted from fetal cells (obtained by amniocentesis or chorionic villus sampling). Main differential diagnoses include Bazex syndrome, trichoepithelioma papulosum multiplex and Torre's syndrome (Muir-Torre's syndrome).Management requires a multidisciplinary approach. Keratocysts are treated by surgical removal. Surgery for BBCs is indicated when the number of lesions is limited; other treatments include laser ablation, photodynamic therapy and topical chemotherapy. Radiotherapy should be avoided. Vitamin A analogs may play a preventive role against development of new BCCs.Life expectancy in NBCCS is not significantly altered but morbidity from complications can be substantial. Regular follow-up by a multi-specialist team (dermatologist, neurologist and odontologist) should be offered. Patients with NBCCS should strictly avoid an excessive sun exposure.
机译:Nevoid基底细胞癌综合征(NBCCS),也称为Gorlin综合征,是一种遗传性疾病,特征在于广泛的发育异常和易患肿瘤。估计患病率从1 / 57,000到1 / 256,000不等,其中男性为女性与女性的比例为1:1;主要临床表现包括多发性基底细胞癌(BCC),颌骨牙源性角化囊肿,手掌和脚底过度角化,骨骼异常,颅内异位钙化和面部畸形(大头畸形,唇left裂/ pal裂)和严重的眼睛异常)。高达5%的病例存在智力缺陷。 BCC(临床上从肉色丘疹到溃疡性斑块不等,直径从1毫米到10毫米不等)通常位于面部,背部和胸部。英国广播公司的数量从几到几千不等。复发性颌骨囊肿发生在90%的患者中。骨骼异常(影响肋骨,椎骨和颅骨的形状)很常见。可能发生眼,泌尿生殖系统和心血管疾病。约有5-10%的NBCCS患者发展为脑恶性髓母细胞瘤,这可能是早期死亡的潜在原因。NBCCS是由PTCH1基因突变引起的,并以常染色体显性性状传播,具有完全的渗透性和可变的表达性。临床诊断依赖于特定标准。基因突变分析证实了诊断。遗传咨询是强制性的。可以通过超声扫描和分析从胎儿细胞中提取的DNA(通过羊膜穿刺术或绒毛膜绒毛取样获得)来进行产前诊断。主要的鉴别诊断包括Bazex综合征,多发性上皮三叉神经瘤和Torre综合征(Muir-Torre综合征)。管理需要采取多学科的方法。角膜囊肿可通过外科手术去除。当病灶数量有限时,需要进行BBC手术。其他治疗方法包括激光消融,光动力疗法和局部化疗。应避免放疗。维生素A类似物可能对新BCC的发生起预防作用.NBCCS的预期寿命没有显着改变,但并发症的发病率可能很高。应该由多专家小组(皮肤科医生,神经科医生和牙科学专家)提供定期随访。 NBCCS患者应严格避免过度日晒。

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