This article was automatically translated from the original Turkish version.
Apocrine sweat glands are specialized sweat glands located particularly in the axillae, groin, and around the mammary region. These glands become active from puberty onward, and their secretions can interact with bacteria on the skin surface, potentially leading to smell formation. Apocrine sweat gland disorders encompass a group of conditions characterized by excessive activity, insufficient activity, or abnormal secretion production by these glands.
Unlike eccrine sweat glands, apocrine sweat glands are larger in structure and their secretions are rich in protein and lipid. These glands are controlled by sympathetic nervous system and become active in response to emotional stress, temperature changes, and hormonal factors.
Apocrine sweat glands originate in the deep layers of the epidermis and are associated with hair follicles. Their secretions reach the skin surface directly through the hair shafts. The cells within these glands operate via an apocrine secretion mechanism, distinct from the merocrine mechanism; that is, a portion of the cell cytoplasm is released along with the secretion together.
Disorders related to apocrine sweat glands typically manifest as excessive sweating (hyperhidrosis), unpleasant odor (bromhidrosis), or inflammation (hidradenitis suppurativa).
Hyperhidrosis is a condition resulting from overactivity of apocrine sweat glands. It is most prominently observed in the axillary and groin regions. Primary hyperhidrosis develops in association with genetic factors, while secondary hyperhidrosis may be linked to hormonal changes or certain systemic diseases.
Bromhidrosis is characterized by the development of unpleasant odor due to bacterial breakdown of apocrine gland secretions. This situation typically arises as a result of poor hygiene and can lead to psychosocial road.
Hidradenitis suppurativa is a chronic inflammatory disease of the apocrine sweat glands. It presents with painful nodules, abscesses, and fistulas, particularly in the axillary and groin regions. Disease typically arises from the interaction of genetic and environmental factors.
The diagnosis of apocrine sweat gland disorders is based on clinical examination and patient history. The following methods may be used to support diagnosis:
The treatment of apocrine sweat gland disorders includes medical and surgical approaches. Treatment selection depends on disease severity, the patient’s overall health status, and its impact on quality of life.
Shelley, W. B., and Hurley, H. J. *Apocrine Glands and Their Disorders*. New York: Academic Press, 1988. Jemec, G. B. E., Revuz, J., and Leyden, J. J. *Hidradenitis Suppurativa*. Springer, 2006. Sato, K., Kang, W. H., Saga, K., and Sato, K. *Biology of Sweat Glands and Their Disorders*. CRC Press, 1999. Burgess, L. *Management of Hyperhidrosis and Bromhidrosis*. Cambridge University Press, 2014. Goldsmith, L. A., Katz, S. I., Gilchrest, B. A., Paller, A. S., Leffell, D. J., and Wolff, K. *Fitzpatrick’s Dermatology in General Medicine*. McGraw-Hill, 2012.
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Anatomy and Physiology of Apocrine Sweat Glands
Structure of Apocrine Sweat Glands
Functions of Apocrine Sweat Glands
Apocrine Sweat Gland Disorders and Clinical Features
Hyperhidrosis
Bromhidrosis
Hidradenitis Suppurativa
Stages of Hidradenitis Suppurativa
Diagnostic Methods
Treatment Methods
Medical Treatment
Surgical Treatment