Williams Abhilasha, Chandrashekar Laxmisha, Srivastava Vivi M, Thomas Meera, Horo Saban, George Renu
Department of Dermatology, Christian Medical College, Ludhiana, Punjab, India.
Department of Dermatology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, Tamil Nadu, India.
Indian J Pathol Microbiol. 2017 Jul-Sep;60(3):424-426. doi: 10.4103/IJPM.IJPM_91_16.
Incontinentia pigmenti (IP) is a rare X-linked dominant disorder, in which skin lesions distributed along Blaschko's lines appear shortly after birth. Early lesions which are erythematous/bullous evolve over time into warty lesions, hyperpigmented swirls/macules, and atrophic hypopigmented streaks. Clinical features are heterogeneous. Abnormalities of the teeth, nails, hair, eyes, central nervous system, and breast may also be present. While intelligence is generally normal, varied degrees of intellectual disability/developmental delay have been reported. Lifespan is normal. IP is associated with mutations of the inhibitor of kappa light polypeptide gene enhancer in B cell, kinase gamma (IKBKG) gene on chromosome Xq28. This gene is involved in the activation of nuclear factor kappa B which protects cells against apoptosis; therefore, cells with IKBKG mutations are extremely susceptible to apoptosis. X-linked dominant disorders are lethal to male fetuses. Males who survive with IP either have mosaicism or an additional X chromosome (Klinefelter syndrome). We present a 22-month-old boy with IP and Klinefelter syndrome.
色素失禁症(IP)是一种罕见的X连锁显性疾病,出生后不久沿布拉斯科线分布的皮肤病变就会出现。早期的红斑/水疱性病变会随着时间的推移演变成疣状病变、色素沉着过度的漩涡/斑疹以及萎缩性色素减退条纹。临床特征具有异质性。牙齿、指甲、头发、眼睛、中枢神经系统和乳房也可能出现异常。虽然智力通常正常,但也有不同程度的智力残疾/发育迟缓的报道。寿命正常。IP与位于Xq28染色体上的B细胞κ轻链多肽基因增强子抑制因子、激酶γ(IKBKG)基因突变有关。该基因参与核因子κB的激活,保护细胞免受凋亡;因此,携带IKBKG突变的细胞极易发生凋亡。X连锁显性疾病对男性胎儿是致命的。患有IP的存活男性要么是嵌合体,要么有一条额外的X染色体(克兰费尔特综合征)。我们报告一例患有色素失禁症和克兰费尔特综合征的22个月大男孩。