107
Views
0
CrossRef citations to date
0
Altmetric
CASE REPORT

Comprehensive Treatment and Gene Analysis of a Male Patient with Follicular Occlusion Tetrad with Fordyce Granules

, ORCID Icon, ORCID Icon & ORCID Icon
Pages 279-285 | Received 20 Oct 2023, Accepted 25 Jan 2024, Published online: 31 Jan 2024

References

  • Sabat R, Jemec GBE, Matusiak Ł, Kimball AB, Prens E, Wolk K. Hidradenitis suppurativa. Nat Rev Dis Primers. 2020;6(1):18. PMID: 32165620. doi:10.1038/s41572-020-0149-1
  • Diajil AR, Goodson ML. Blood group in relation to oral Fordyce’s granules and serum cholesterol level. J Oral Pathol Med. 2023;52(6):521–527. PMID: 37038041. doi:10.1111/jop.13432
  • De Felice C, Parrini S, Chitano G, Gentile M, Dipaola L, Latini G. Fordyce granules and hereditary non-polyposis colorectal cancer syndrome. Gut. 2005;54(9):1279–1282. PMID: 15879014; PMCID: PMC1774669. doi:10.1136/gut.2005.064881
  • Pillsbury DM, Shelley WB, Kligman AM. Dermatology. Vol. 482–484. Philadelphia: Saunders; 1956:489.
  • Plewig G, Kligman AM. Acne. Morphogenesis and Treatment. Berlin: Springer; 1975:192–193.
  • Plewig G, Steger M. Acne inversa (alias acne triad, acne tetrad or hidradenitis suppurativa). In: Marks R, Plewig G, editors. Acne and Related Disorders. London: Martin Dunitz; 1989:345–357.
  • Atzori L, Zanniello R, Pilloni L, Rongioletti F. Steatocystoma multiplex suppurativa associated with hidradenitis suppurativa successfully treated with Adalimumab. J Eur Acad Dermatol Venereol. 2019;33(Suppl 6):42–44. PMID: 31535759. doi:10.1111/jdv.15848
  • Jemec GB. Clinical practice. Hidradenitis suppurativa. N Engl J Med. 2012;366(2):158–164. PMID: 22236226. doi:10.1056/NEJMcp1014163
  • Wang B, Yang W, Wen W, et al. Gamma-secretase gene mutations in familial acne inversa. Science. 2010;330(6007):1065. doi:10.1126/science.1196284
  • Yan J, Zhang G, Liao C, Wang X, Shi L. ALA-iPDT for follicular occlusion tetrad concomitant with pachyonychia congenital type II and ankylosing spondylitis. Photodiagnosis Photodyn Ther. 2022;39:102891. PMID: 35490959. doi:10.1016/j.pdpdt.2022.102891
  • Tummala H, Walne A, Collopy L, et al. Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita. J Clin Invest. 2015;125(5):2151–2160. PMID: 25893599; PMCID: PMC4463202. doi:10.1172/JCI78963
  • Walne AJ, Vulliamy T, Kirwan M, Plagnol V, Dokal I. Constitutional mutations in RTEL1 cause severe dyskeratosis congenita. Am J Hum Genet. 2013;92(3):448–453. PMID: 23453664; PMCID: PMC3591859. doi:10.1016/j.ajhg.2013.02.001
  • Altunay IK, Gökdemir G, Kurt A, Kayaoglu S. Hidradenitis suppurativa and squamous cell carcinoma. Dermatol Surg. 2002;28(1):88–90. PMID: 11991278. doi:10.1046/j.1524-4725.2002.01090.x
  • Borowiec M, Liew CW, Thompson R, et al. Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction. Proc Natl Acad Sci U S A. 2009;106(34):14460–14465. PMID: 19667185; PMCID: PMC2732833. doi:10.1073/pnas.0906474106
  • Zhang Y, Fang X, Wei J, et al. PDX-1: a promising therapeutic target to reverse diabetes. Biomolecules. 2022;12(12):1785. PMID: 36551213; PMCID: PMC9775243. doi:10.3390/biom12121785
  • Trebusak Podkrajsek K, Tesovnik T, Bozanic Urbancic N, Battelino S. Novel GRHL2 gene variant associated with hearing loss: a case report and review of the literature. Genes. 2021;12(4):484. PMID: 33810548; PMCID: PMC8066333. doi:10.3390/genes12040484
  • Vona B, Nanda I, Neuner C, Müller T, Haaf T. Confirmation of GRHL2 as the gene for the DFNA28 locus. Am J Med Genet A. 2013;161A(8):2060–2065. PMID: 23813623; PMCID: PMC3884766. doi:10.1002/ajmg.a.36017