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Cutaneous meningioma

Cutaneous meningioma, also known as heterotopic meningeal tissue, and rudimentary meningocele is a developmental defect, and results from the presence of meningocytes outside the calvarium.

Signs and symptoms
Lesions appear as hard, subcutaneous lumps that might be pale or somewhat black in appearance. Alopecic lesions with overlaying hair tufts or even hypertrichosis have been reported. Although usually painless, some people have reported experiencing discomfort or tenderness. == Causes ==
Causes
While type II and type III tumors form later in life, type I tumors are congenital. == Diagnosis ==
Diagnosis
Since imaging studies and clinical characteristics are frequently equivocal, cytology, and particularly histology, is essential for determining the final diagnosis. Meningothelial cells arranged in a whorled pattern with lobules, nests, and sheets of oval or polygonal cells are the most prevalent histopathological form. These cells display calcification foci (psammomma bodies) or hyaline structures (collagen bodies), which are highly useful diagnostic markers. • Ectopic soft tissue meningioma around the eyes, ears, nose, and mouth that spreads to the skin by contiguity. There are no known related meningiomas of neuraxis. • Adult cases of neuroaxis-related meningioma tumors that spread to the dermis and subcutaneous tissue are significantly more common. They could result from trauma, any other surgical cause, or a bone deformity. == Treatment ==
Treatment
Complete surgical excision is the basis of treatment. == See also ==
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