KID Syndrome Complicated by Multiple Abscesses of the Parietal Region Skin: Clinical Case
https://doi.org/10.15690/vsp.v20i1.2240
Abstract
Background. KID syndrome (keratitis-ichthyosis-deafness) is an orphan genetic multisystem disease with autosomal recessive and dominant types of inheritance, it manifests in the neonatal period. The leading triad of symptoms is: skin lesions, ophthalmological diseases and hearing organ pathology. Clinical Case Description. Girl V., 17 years old, with KID syndrome applied to the hospital complaining on painful infiltrates of the parietal region. Multiple abscesses were lanced. Hyperkeratotic crusts were removed, unviable skin regions were excised, and abscesses' cavities were washed with antiseptic solution during daily dressings. Purulent discharge from wounds has been maintaining for 7 days. Conclusion. Where is no pathogenetic treatment for KID syndrome yet. Prevention of secondary surgical infections remains the crucial aspect in the management of such patients. Local wound treatment, symptomatic and antibacterial therapy are effective in case of skin infection.
About the Authors
Anastasia A. BebeninaRussian Federation
Moscow.
Disclosure of interest:
Not declared.
Madina A. Chundokova
Russian Federation
Moscow.
Disclosure of interest:
Not declared.
Alexey N. Smirnov
Russian Federation
Moscow.
Disclosure of interest:
Not declared.
Maxim A. Golovanev
Russian Federation
Moscow.
Disclosure of interest:
Not declared.
Alina A. Dokshukina
Russian Federation
Moscow.
Disclosure of interest:
Not declared.
References
1. Lyashenko NV, Kolyaseva NA. KID syndrome: congenital ichthyosiform erythroderma with deafness and keratitis. Health, Demography, Ecology of Finno-Ugric People. 2016;(4):39-41. (In Russ).
2. Markova TG, Brazhkina NB, Bliznets EA, et al. Diagnostics of keratitis-ichthyosis-deafness syndrome (KID-syndrome). Vestnik otorinolaringologii = Bulletin of Otorhinolaryngology. 2012;(3):58-61. (In Russ).
3. Gonzalez ME, Tlougan BE, Price HN, et al. Keratitis-ichthyosis-deafness (KID) syndrome. Dermatol Online J. 15;(8):11.
4. Dey VK, Saxena A, Parikh S. KID Syndrome: A Rare Geno-dermatosis. Indian Dermatol Online J. 2020;11(1):116-118. doi: 10.4103/idoj.IDOJ_87_19
5. Klymenko VA, Zdybska OP, Sirenko TV, et al. Clinical observation of a child with KID (keratitis-ichthyosis-deafness) syndrome. Child's Health. 2015;6(66):129-132. (In Russ).
6. Abdollahi A, Hallaji, Esmaili N, et al. KID syndrome. Dermatol Online J. 2007;13(4):11.
7. Coggshall K, Farsani T, Ruben B, et al. Keratitis, ichthyosis, and deafness (KID) syndrome: a review of infectious and neoplastic complications. J Am Acad Dermatol. 2013;69(1):127-134. doi: 10.1016/j.jaad.2012.12.965
8. Jovanovic D, Paravina M, Stanojevic M, et al. Keratitis, ichthyosis and deafness (KID) syndrome: case study. Acta Med Median. 1998;5:67-72.
9. Stepanovic M, Paravina M, Jankovic, Janjic Spasic D. Keratitis, Ichthyosis and Deafness (KID) Syndrome — a Case Report. Serbian J Dermatol Venereol. 2013;5(1):22-30. doi: 10.2478/sjdv-2013-0003
10. Alli N, Gungor E. Keratitis, ichthyosis and deafness (KID) syndrome. Int J Dermatol. 1997;36:37-40.
11. Kapila A, De Baerdemaeker R, Bakal F, et al. A Rare Case of KID Syndrome: The Use of Hydrosurgery and Strategies for Antiseptic Wound Care. Adv Skin Wound Care. 2019;32(10):1-6. doi: 10.1097/01.ASW.0000580480.86585.3a
12. Murashkin NN, Ambarchyan ET, Epishev RV, Materikin AI. Skin barrier properties in norm and pathology. Pediatria n.a. G.N. Speransky. 2015;94(6):165-169. (In Russ).
13. Gostishchev V.K. Obshchaya khirurgiya: Textbook. — 4th ed. upd. and rev. Moscow: GEOTAR-media; 2010. 848 p. (In Russ).
Review
For citations:
Bebenina A.A., Chundokova M.A., Smirnov A.N., Golovanev M.A., Dokshukina A.A. KID Syndrome Complicated by Multiple Abscesses of the Parietal Region Skin: Clinical Case. Current Pediatrics. 2021;20(1):67-71. (In Russ.) https://doi.org/10.15690/vsp.v20i1.2240