Bullous aplasia cutis congenita - a report of two cases and brief review of the literature

被引:0
|
作者
Prcic, Sonja [1 ,4 ]
Matic, Aleksandra [1 ,4 ]
Jablanovic, Sladjana [1 ]
Matic, Milan [2 ,4 ]
Gajinov, Zorica [2 ,4 ]
Stasuk, Natasa [3 ]
机构
[1] Inst Child & Youth Hlth Care Vojvodina, Pediat Clin, Hajduk Veljkova 10, Novi Sad 21000, Serbia
[2] Clin Ctr Vojvodina, Clin Dermatovenereol Dis, Novi Sad, Serbia
[3] Clin Ginecol & Obstest, Novi Sad, Serbia
[4] Univ Novi Sad, Fac Med, Novi Sad, Serbia
关键词
congenital abnormalities; ectodermal dysplasia; scalp; hypertrichosis; hemangioma; SKIN;
D O I
10.2298/VSP170201076P
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction. Aplasia cutis congenita (ACC) is a rare condition characterized by the focal absence of skin, and sometimes other underlying structures at birth. It may occur as an isolated defect or associated with other anomalies and defects. Bullous ACC (BACC) is a clinical subtype of the condition with few cases reported in the literature. It presents as a bullous lesion at birth which gradually transforms into an atrophic scar covered by a thin epithelial membrane. It is considered as cutaneous sign of possible neural tube dysraphism. Some cases present with a dark hair around the lesion (the hair collar sign), which can be even more indicative of neural tube defect. However, cases of BACC reported till today are inconclusive regarding this connection. Case report. We report a two cases of BACC of the scalp, in one patient associated with hair collar sign without neural tube defects and the other with hemangioma and we give a brief review of the selected literature. Conclusion. Bullous or membranous aplasia cutis congenita is benign condition, but may represent as a cutaneous marker of occult neural tube defect. Recognising the condition is important in order to rule out associated anomalies.
引用
收藏
页码:345 / 348
页数:4
相关论文
共 50 条
  • [1] Aplasia cutis congenita: Report of four cases and literature review
    Loreti A.
    Bracaglia R.
    Selvaggi G.
    Lahoud P.
    Sturla M.
    Farallo E.
    European Journal of Plastic Surgery, 2004, 27 (3) : 114 - 119
  • [2] Isolated aplasia cutis congenita: A report of two cases
    Wu, Yan
    Liu, Jun
    Luo, Qiong
    CLINICAL CASE REPORTS, 2021, 9 (08):
  • [3] Aplasia cutis congenita: A case report and literature review
    Duan, Xunhong
    Yang, Ge
    Yu, Dongqi
    Yu, Changlong
    Wang, Biao
    Guo, Yibin
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2015, 10 (05) : 1893 - 1895
  • [4] Bullous aplasia cutis congenita
    Colon-Fontanez, F
    Friedlander, SF
    Newbury, R
    Eichenfield, LF
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2003, 48 (05) : S95 - S98
  • [5] Aplasia cutis congenita: a report of two cases from National Hospital Abuja, Nigeria and review of the literature
    Mukhtar-Yola, Mariya
    Mshelia, Lauretta
    Mairami, Amsa
    Otuneye, Adekunle Tolutope
    Yawe, Edith Terna
    Igoche, Patricia
    Audu, Lamidi Isah
    PAN AFRICAN MEDICAL JOURNAL, 2020, 36 : 1 - 9
  • [6] Abdominal aplasia cutis congenita: Case report and review of the literature
    Verhelle, NAC
    Heymans, O
    Deleuze, JP
    Fabre, G
    Vranckx, JJ
    Van den Hof, B
    JOURNAL OF PEDIATRIC SURGERY, 2004, 39 (02) : 237 - 239
  • [7] Systemic aplasia cutis congenita: A case report and review of the literature
    Zhou, Juan
    Zheng, Li
    Tao, Wenqi
    PATHOLOGY RESEARCH AND PRACTICE, 2010, 206 (07) : 504 - 507
  • [8] Dermoscopy of Aplasia Cutis Congenita: A Case Report and Review of the Literature
    Neelam, Rasna
    Nakamura, Mio
    Tejasvi, Trilokraj
    DERMATOLOGY PRACTICAL & CONCEPTUAL, 2021, 11 (01):
  • [9] Aplasia cutis congenita with fetus papyraceus: report and review of the literature
    Tempark, Therdpong
    Shwayder, Tor A.
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2012, 51 (12) : 1419 - 1426
  • [10] Aplasia cutis congenita: report of 22 cases
    Mesrati, Hela
    Amouri, Meriem
    Chaaben, Hend
    Masmoudi, Abdelrahmen
    Boudaya, Sonia
    Turki, Hamida
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54 (12) : 1370 - 1375