Dermatofibromahttps://en.wikipedia.org/wiki/Dermatofibroma
Dermatofibroma huwa papules solitarji iebsa li jikbru bil-mod (ħotob fit-tond) li normalment kannella għal kannella; Għalkemm dermatofibromas tipiċi jikkawżaw ftit jew xejn skumdità, jistgħu jseħħu ħakk u sensittività. Dermatofibromas jistgħu jinstabu kullimkien fuq il-ġisem, iżda ħafna drabi jinstabu fuq is-saqajn u l-dirgħajn.

Dermatofibromas jistgħu jiġu ffurmati bħala reazzjoni għal korrimenti preċedenti bħal gdim ta 'insetti jew pricks tax-xewk. Dermatofibromas huma kklassifikati bħala leżjonijiet beninni tal-ġilda, li jfisser li huma kompletament bla ħsara, għalkemm Dermatofibromas jistgħu jiġu konfużi ma 'varjetà ta' tumuri taħt il-ġilda. Dermatofibromas penetranti fil-fond jistgħu jkunu diffiċli biex jiġu distinti, anke istoloġikament, minn tumuri fibroistoċitiċi malinni rari bħal "dermatofibrosarcoma protuberans".

Djanjosi u Trattament
Ħafna huma beninni, iżda leżjonijiet kbar (>5 mm) jistgħu jeħtieġu bijopsija.
#Dermoscopy
#Skin biopsy
☆ Fir-riżultati ta' Stiftung Warentest tal-2022 mill-Ġermanja, is-sodisfazzjon tal-konsumatur b'ModelDerm kien biss ftit inqas milli b'konsultazzjonijiet bit-telemediċina mħallsa.
  • Każ tipiku ta' Dermatofibroma ― Nodulu iebes fuq ir-riġlejn. Dermatofibroma huwa tumur benin relattivament komuni.
References Dermatofibroma 29262213 
NIH
Dermatofibroma hija kundizzjoni komuni tal-ġilda li tinsab l-aktar fuq id-dirgħajn jew ir-riġlejn. Jidher bħala ċapep sodi taħt il-ġilda, ħafna drabi inqas minn ċentimetru fid-daqs. Filwaqt li normalment bla tbatija, jista 'jkun marbut ma' korrimenti minuri tal-passat bħal gdim ta 'insetti jew pricks tax-xewk. Dermatofibromas jistgħu jaffettwaw lil kulħadd iżda huma aktar komuni fin-nisa ta 'età minn 20 sa 40. Huma tipikament beninni, iżda xi drabi jistgħu jerġgħu lura wara t-tneħħija. Huwa importanti li tiddifferenzja dermatofibromas minn tumur tal-ġilda aktar aggressiv imsejjaħ dermatofibrosarcoma protuberans.
Dermatofibroma is a commonly occurring cutaneous entity usually centered within the skin's dermis. Dermatofibromas are referred to as benign fibrous histiocytomas of the skin, superficial/cutaneous benign fibrous histiocytomas, or common fibrous histiocytoma. These mesenchymal cell lesions of the dermis clinically are firm subcutaneous nodules that occur on the extremities in the vast majority of cases and may or may not be associated with overlying skin changes. They are most commonly asymptomatic and usually relatively small, less than or equal to 1 centimeter in diameter. Often, patients who present with a dermatofibroma relate a history of possibly inciting local trauma at the site, such as from an insect bite or superficial puncture wound from thorns or wood splinters. Dermatofibromas occur in people of all ages, although more commonly during the ages of the 20s to 40s, and develop more frequently in females than males, with as high as a 2:1 female to male predominance according to some reports. They are a benign tumor, although there have been cases of local recurrence, and even more rarely, distant metastases have been reported. When considering the differential diagnosis of these lesions, it is vitally important to distinguish dermatofibromas from dermatofibrosarcoma protuberans, a similar-appearing but more aggressive cutaneous neoplasm.
 Common Benign Skin Tumors 12613727
It-trattament preferut għal lipomas, dermatofibromas, keratoacanthomas, pyogenic granulomas, epidermoid cysts huwa t-tneħħija kirurġika. Cherry angiomas, sebaceous hyperplasia huma ttrattati b'mod komuni b'terapija bil-laser jew elettrodessikazzjoni. Il-krijoterapija u t-tneħħija tal-leħja huma għażliet popolari għal acrochordons, seborrheic keratoses. Jekk tabib tal-familja jħossu inċert dwar id-dijanjosi jew it-trattament ta 'leżjoni, jew jekk bijopsija tikkonferma melanoma, riferiment għal speċjalista huwa rakkomandat.
The preferred treatment for lipomas, dermatofibromas, keratoacanthomas, pyogenic granulomas, epidermoid cysts is surgical removal. Cherry angiomas, sebaceous hyperplasia are commonly treated with laser therapy or electrodesiccation. Cryotherapy and shave excision are popular choices for acrochordons, seborrheic keratoses. If a family physician feels uncertain about diagnosing or treating a lesion, or if a biopsy confirms melanoma, referral to a specialist is recommended.