Rokunohe Akiko, Nakano Hajime, Aizu Takayuki, Kaneko Takahide, Nakajima Koji, Ikenaga Satsuki, Matsuzaki Yasushi, Murai Takaya, Tamai Katsuto, Sawamura Daisuke
Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
J Dermatol. 2008 Jun;35(6):336-40. doi: 10.1111/j.1346-8138.2008.00479.x.
The most life-threatening complication developing in patients with recessive dystrophic epidermolysis bullosa (RDEB) is squamous cell carcinoma (SCC). To improve patient prognosis, early detection of regional lymph node metastasis is required. Herein, we report a patient diagnosed with non-Hallopeau-Siemens RDEB who developed SCC on the left foot with inguinal lymph node swelling. Use of the sentinel node biopsy (SNB) technique favorably minimized defective damage to the inguinal region in this case. Genetic analysis identified one novel COL7A1 mutation, a maternal c.238G > C (p.A80P) and one previously reported mutation, a paternal c.3631C > T (p.Q1211X). A published work review demonstrated that no COL7A1 mutations specific for SCC development in RDEB have previously been identified. It remains unclear if SNB in combination with gene diagnosis is beneficial for the management of SCC in RDEB patients, however, because of the limited number of case reports. To address this issue, COL7A1 mutational analysis should be performed in as many cases of RDEB as possible.
隐性营养不良型大疱性表皮松解症(RDEB)患者最危及生命的并发症是鳞状细胞癌(SCC)。为改善患者预后,需要早期检测区域淋巴结转移。在此,我们报告一例被诊断为非Hallopeau-Siemens型RDEB的患者,其左脚出现SCC并伴有腹股沟淋巴结肿大。在该病例中,前哨淋巴结活检(SNB)技术的应用成功将腹股沟区域的缺损损伤降至最低。基因分析鉴定出一个新的COL7A1突变,即母亲的c.238G > C(p.A80P),以及一个先前报道的突变,即父亲的c.3631C > T(p.Q1211X)。一项已发表的文献综述表明,此前尚未发现RDEB中SCC发生所特有的COL7A1突变。然而,由于病例报告数量有限,尚不清楚SNB联合基因诊断对RDEB患者SCC的管理是否有益。为解决这一问题,应在尽可能多的RDEB病例中进行COL7A1突变分析。