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2.
Dermatol Online J ; 20(7)2014 Jul 15.
Article in English | MEDLINE | ID: mdl-25046461

ABSTRACT

Pilomatrix carcinoma is a rare malignant tumor that originates from hair matrix cells. It is not usually considered in a differential diagnosis owing to its low incidence. We present a case of this uncommon entity and review the literature.


Subject(s)
Facial Neoplasms/diagnosis , Hair Diseases/diagnosis , Skin Neoplasms/diagnosis , Aged, 80 and over , Biopsy , Diagnosis, Differential , Humans , Male
11.
Lasers Med Sci ; 26(3): 285-90, 2011 May.
Article in English | MEDLINE | ID: mdl-21347722

ABSTRACT

BACKGROUND: Angiolymphoid hyperplasia with eosinophilia is a rare, benign disorder characterized by reddish-brown nodules and plaques in the dermis and the subcutaneous tissues, typically occurring on the neck and head. Surgical excision, corticosteroids, radiotherapy, and other therapies have been used, however, recurrences are common. Treatment with vascular lasers such as pulsed dye laser (PDL) or Nd:YAG seems to be a promising therapeutic option. OBJECTIVE: To assess the efficacy and safety of PDL and combined sequential PDL-Nd:YAG laser in patients with ALHE. METHODS: Three patients with ALHE were treated with PDL at 595-nm wavelength or with a combined sequential application of 595-nm PDL and 1,064-nm Nd:YAG wavelengths. Topical anesthetic was applied before laser treatment. RESULTS: Complete resolution of the lesions was achieved in two patients with ALHE; a partial response was seen in one patient. No significant side-effects were reported. CONCLUSIONS: We consider that PDL should be a first-line therapy for AHLE. Sequential application of PDL and Nd:YAG laser seems to show promising results, so it could be an interesting new treatment option.


Subject(s)
Angiolymphoid Hyperplasia with Eosinophilia/surgery , Lasers, Dye/therapeutic use , Adult , Aged , Angiolymphoid Hyperplasia with Eosinophilia/pathology , Ear , Female , Humans , Remission Induction , Treatment Outcome , Young Adult
12.
Dermatol Online J ; 16(12): 14, 2010 Dec 15.
Article in English | MEDLINE | ID: mdl-21199640

ABSTRACT

Cutis verticis gyrata is a rare skin condition characterized by ridges and furrows resembling the surface of the brain. It can be considered as a manifestation of a variety of diverse causes such as cerebriform intradermal nevus. We report a 48-year-old man with cerebriform and soft folds on the left parietal and temporal areas. Histology showed solitary or clusters of nevus cells in the dermis. The diagnosis of cerebriform intradermal nevus was confirmed.


Subject(s)
Head and Neck Neoplasms/diagnosis , Nevus, Intradermal/diagnosis , Scalp Dermatoses/etiology , Scalp , Skin Neoplasms/diagnosis , Alopecia Areata/etiology , Diagnosis, Differential , Head and Neck Neoplasms/complications , Humans , Male , Melanosis/diagnosis , Melanosis/etiology , Middle Aged , Neurocutaneous Syndromes/diagnosis , Nevus, Intradermal/complications , Scalp/pathology , Skin Neoplasms/complications
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