Histoid leprosy explained

Specialty:Dermatology

Histoid leprosy is a skin condition, a rare form of multibacillary leprosy.[1] It can occur in those with relapsing leprosy after undergoing antibiotic therapy with dapsone, or less frequently in the first infection (termed de novo).[2]

Leprosy can appear in two forms, tuberculoid leprosy and lepromatous leprosy, and histoid leprosy is a variant of lepromatous leprosy. It appears as "cutaneous and/or subcutaneous nodules and papules, which are painless, succulent, discrete, smooth, globular, skin-colored to yellowish-brown, with apparently normal skin surrounding it."[3] In India, histoid leprosy is estimated to compose 2.79%-3.6% of all leprosy cases. The male to female ratio in most parts of the world is 2:1. It is treated with antimycobacterial chemotherapy and multibacillary multidrug therapy.

See also

Notes and References

  1. Book: James, William D. . Berger, Timothy G. . Andrews' Diseases of the Skin: clinical Dermatology . Saunders Elsevier . 2006 . 0-7216-2921-0 . etal.
  2. Pandey . Pooja . Suresh . Mavinrkainahalli Srinivasa Murthy . Dey . Vivek Kumar . 2015 . De Novo Histoid Leprosy . Indian Journal of Dermatology . 60 . 5 . 525 . 10.4103/0019-5154.159666 . 1998-3611 . 4601467 . 26538746 . free.
  3. Gupta . Sunil Kumar . 2015-06-20 . Histoid leprosy: review of the literature . International Journal of Dermatology . 54 . 11 . 1283–1288 . 10.1111/ijd.12799 . 0011-9059.