Chromhidrosis

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Chromhidrosis
Other namesColored sweat [1]
Skin.png
Specialty Dermatology

Chromhidrosis is a rare condition characterized by the secretion of colored sweat. [2] It is caused by the deposition of lipofuscin in the sweat glands. Cases of red, blue, green, yellow, pink, and black sweat have been reported.[ by whom? ]

Contents

Usually, chromhidrosis affects the apocrine glands, mainly on the face and underarms. A limited number of treatment options exist, including regular application of capsaicin cream, and prolonged relief may be provided by botulinum toxin treatment. Chromogenic pigments produced by bacteria ( Corynebacterium in particular) are implicated in this condition, but their exact role still requires careful microbiological elucidation.

Chromhidrosis of the eccrine glands is rare; it occurs mainly after the ingestion of certain dyes or drugs.

See also

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Eccrine sweat gland Sweat gland distributed almost all over the human body

Eccrine sweat glands are the major sweat glands of the human body, found in virtually all skin, with the highest density in palm and soles, then on the head, but much less on the torso and the extremities. In other mammals, they are relatively sparse, being found mainly on hairless areas such as foot pads. They reach their peak of development in humans, where they may number 200–400/cm2 of skin surface. They produce a clear, odorless substance, sweat, consisting primarily of water. These are present from birth. Their secretory part is present deep inside the dermis.

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Hidradenitis is any disease in which the histologic abnormality is primarily an inflammatory infiltrate around the eccrine glands. This group includes neutrophilic eccrine hidradenitis and recurrent palmoplantar hidradenitis.

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Idiopathic pure sudomotor failure (IPSF) is the most common cause of a rare disorder known as acquired idiopathic generalized anhidrosis (AIGA), a clinical syndrome characterized by generalized decrease or absence of sweating without other autonomic and somatic nervous dysfunctions and without persistent organic cutaneous lesions.

References

  1. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10th ed.). Saunders. p. 179. ISBN   978-0-7216-2921-6.
  2. Freedberg, Irwin M.; Eisen, Arthur Z.; Wolff, Klauss; Austen, K. Frank; Katz, Lowell A.; Katz, Stephen, eds. (2003). Fitzpatrick's Dermatology in General Medicine (6th ed.). New York: McGraw-Hill. p. 708. ISBN   978-0-07-138076-8.

Further reading

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