Severe acquired ichthyosis due to autoimmune thyroiditis: therapeutic response to thyroxine replacement therapy

Authors

  • Chandramohan Kudligi
  • Pradeep Vittal Bhagwat
  • Arun Thirunavukkarasu
  • Mohan Shendre Eshwar Rao
  • Dr. Suphala B

DOI:

https://doi.org/10.66344/jpad.21.2.2011.457

References

Kuokkanen K. Ichthyosis vulgaris. A clinical and histopathological study of patients and their close relatives in the autosomal dominant and sex-linked forms of the disease. Acta Derm Venereol 1969; 62: 1-72.

Wells RS, Kerr CB. Clinical features of autosomal dominant and sex-linked ichthyosis in an English population. Br Med J 1966; 1: 947-50.

Schwartz RA, Williams ML. Acquired ichthyosis: a marker for internal disease. Am Fam Physician 1984; 29: 181-4.

Tlacuilo-Parra JA, Guevara-Gutierrez E, Salazar-Paramo M. Acquired ichthyosis associated with systemic lupus erythematosus. Lupus 2004; 13: 270-3.

Okulicz J, Schwartz R. Hereditary and acquired ichthyosis vulgaris. Int J Dermatol 2003; 42: 95-8.

Patel N, Spencer LA, English JC 3rd, Zirwas MJ. Acquired ichthyosis. J Am Acad Dermatol 2006; 55: 647-56.

Aram H. Acquired ichthyosis and related conditions. Int J Dermatol 1984; 23: 458-61.

Brazzelli V, Prestinari F, Barbagallo T et al. Acquired ichthyosis and hypertrichosis due to autoimmune thyroiditis: therapeutic response to thyroxine replacement. Pediatr Dermatol 2005; 22: 447-9.

Downloads

Published

2016-12-22

How to Cite

1.
Kudligi C, Bhagwat PV, Thirunavukkarasu A, Eshwar Rao MS, Suphala B D. Severe acquired ichthyosis due to autoimmune thyroiditis: therapeutic response to thyroxine replacement therapy. J Pak Assoc Dermatol [Internet]. 2016Dec.22 [cited 2026Apr.19];21(2):128-9. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/457

Issue

Vol. 21 No. 2 (2011): April - June

Section

Short Communications

License

Submission declaration

Authors retain the copyright to their work and grant the 'Journal of Pakistan Association of Dermatologists (JPAD)' the right of first publication under a Creative Commons Attribution 4.0 International (CC BY 4.0) license. This license allows others to share, adapt, and reuse the work for any purpose, including commercial use, as long as appropriate credit is given to the original authors and the journal.

By submitting a manuscript, authors confirm that the work has not been published previously (except as an abstract, lecture, or academic thesis), is not under review elsewhere, and has been approved by all authors and relevant authorities. Once accepted, the article will be openly accessible under the CC BY 4.0 license, ensuring wide dissemination and reuse with proper attribution.

Most read articles by the same author(s)

1 2 > >>