Cutaneous myxoma
Cutaneous Myxoma is a rare, benign soft tissue tumor that originates in the skin. It is part of a group of tumors known as myxomas, which are characterized by the presence of mucoid (myxoid) connective tissue. Cutaneous myxomas are most commonly found in adults and can occur anywhere on the body, but they have a predilection for the head, neck, and extremities.
Etiology and Pathogenesis[edit | edit source]
The exact cause of cutaneous myxoma is not well understood. It is believed to be sporadic in most cases, although some may be associated with genetic syndromes such as Carney Complex, a condition characterized by multiple myxomas, skin pigmentation abnormalities, and endocrine overactivity. The pathogenesis involves the proliferation of stellate or spindle-shaped cells within a myxoid stroma, which is rich in hyaluronic acid.
Clinical Features[edit | edit source]
Cutaneous myxoma presents as a solitary, slow-growing, painless, and soft to rubbery nodule. The overlying skin is usually normal in appearance. Lesions are typically less than 2 cm in diameter but can vary in size. Due to their benign nature, cutaneous myxomas do not metastasize but can recur if not completely excised.
Diagnosis[edit | edit source]
The diagnosis of cutaneous myxoma is primarily based on histopathological examination of the excised lesion. Imaging studies are not typically required but may be used to assess the extent of larger or deeper lesions. Histologically, cutaneous myxomas are characterized by a loose, myxoid stroma with scattered spindle-shaped cells and a variable amount of collagen fibers.
Treatment[edit | edit source]
The treatment of choice for cutaneous myxoma is complete surgical excision with clear margins to prevent recurrence. There is no role for chemotherapy or radiation therapy in the treatment of these benign tumors. Follow-up is recommended to monitor for recurrence, especially in cases associated with syndromes that predispose to multiple myxomas.
Prognosis[edit | edit source]
The prognosis for cutaneous myxoma is excellent, with complete excision being curative in most cases. Recurrence is rare but can occur, particularly if the excision is incomplete.
Epidemiology[edit | edit source]
Cutaneous myxoma is a rare condition, and its exact incidence is unknown. It can occur at any age but is most commonly diagnosed in adults. There is no clear gender predilection.
Differential Diagnosis[edit | edit source]
The differential diagnosis for cutaneous myxoma includes other soft tissue tumors such as neurofibroma, lipoma, and dermatofibroma. Histopathological examination is essential for accurate diagnosis.
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD