Steatocystoma multiplex - Steatocistomas Multiplekss
☆ 2022. gada Stiftung Warentest rezultātos no Vācijas patērētāju apmierinātība ar ModelDerm bija tikai nedaudz zemāka nekā ar maksas telemedicīnas konsultācijām.
References
Steatocystoma multiplex (SM) , pazīstama arī kā steatocistomatoze vai epidermas policistiska slimība, ir reta un labdabīga ādas slimība, kam raksturīgas vairākas dažāda lieluma intradermālas tauku cistas. Klīniski SM parādās kā daudzi, gludi, stingri un kustīgi cistiski izciļņi un izciļņi, bieži vien bez jebkādiem simptomiem. Šie bojājumi parasti ir apaļi un vienāda izmēra, svārstās no dažiem milimetriem līdz centimetriem. To virsma var būt dzeltenīga nokrāsa, savukārt dziļākas parasti atbilst ādas krāsai. Šķidrums šajās cistās parasti ir bez smaržas un eļļains, ar dažādu skaidrības un krāsas pakāpi. Atšķirībā no tipiskām cistām, parasti nav redzamas atveres ādas centrā, kas pārklāj cistu. SM var attīstīties jebkurā ķermeņa vietā, bet parasti sastopama reģionos ar bagātīgiem tauku dziedzeriem un matu folikulām, piemēram, stumbrā, kaklā, galvas ādā, padusēs, rokās, kājās un cirkšņos.
Steatocystoma multiplex (SM, also known as steatocystomatosis, sebocystomatosis, or epidermal polycystic disease) is a rare benign intradermal true sebaceous cyst of various sizes. Clinically, SM presents as asymptomatic, numerous, round, smooth, firm, mobile, cystic papules, and nodules. The lesions are uniform, with a size of a few millimeters to centimeters along the long axis. The superficial lesions are yellowish, and deeper lesions tend to be skin-colored. The fluid in SM is odorless, oily, clear or opaque, milky or yellow. The overlying epidermal skin is often normal, with no central punctum. SM can occur anywhere in the body but is more frequently seen in areas rich in pilosebaceous units such as the trunk (especially the presternal region), neck, scalp, axilla, proximal extremities, and inguinal region.
Steatocystoma multiplex (SM, also known as steatocystomatosis, sebocystomatosis, or epidermal polycystic disease) is a rare benign intradermal true sebaceous cyst of various sizes. Clinically, SM presents as asymptomatic, numerous, round, smooth, firm, mobile, cystic papules, and nodules. The lesions are uniform, with a size of a few millimeters to centimeters along the long axis. The superficial lesions are yellowish, and deeper lesions tend to be skin-colored. The fluid in SM is odorless, oily, clear or opaque, milky or yellow. The overlying epidermal skin is often normal, with no central punctum. SM can occur anywhere in the body but is more frequently seen in areas rich in pilosebaceous units such as the trunk (especially the presternal region), neck, scalp, axilla, proximal extremities, and inguinal region.
25 gadus vecs vīrietis ieradies ar ādas stāvokli uz rokām, krūtīm un vēdera. Viņam 20 gadus bija nesāpīgi kunkuļi, sākot no krūtīm un izplatoties uz rokām pēdējo 7 gadu laikā.
A 25-year-old man came in with a skin condition on his arms, chest, and abdomen. He had been with painless lumps for 20 years, starting on his chest and spreading to his arms over the past 7 years.
A 25-year-old man came in with a skin condition on his arms, chest, and abdomen. He had been with painless lumps for 20 years, starting on his chest and spreading to his arms over the past 7 years.
Iesākums pubertātes laikā, domājams, ir saistīts ar hormonālajiem stimuliem pilosebaceous vienībā. Visbiežāk tie rodas uz krūtīm un var rasties arī uz vēdera, augšdelmiem, padusēm un sejas. Dažos gadījumos cistas var attīstīties visā ķermenī.