منابع مشابه
Oral focal mucinosis: report of two cases
a Department of Oral and Maxillofacial Pathology, Pacific Dental College and Hospital, Debari, Udaipur, Rajastan State, India b Department of Oral and Maxillofacial Surgery, SJM Dental College and Hospital, Chitradurga, Karnataka State, India c Department of Oral and Maxillofacial Pathology, KM Shah Dental College and Hospital, Pipariya, Vadodara, Gujarat State, India d Department of Oral and M...
متن کاملLocalized papular mucinosis with IgA nephropathy: a case report.
BACKGROUND Papular mucinosis is an idiopathic cutaneous mucinosis. It includes 3 clinicopathologic subsets according to the recent Rongioletti classification: a generalized papular form, a localized form, and atypical forms. The localized form is subdivided into 5 subtypes. The atypical form does not meet the criteria for either the generalized papular form or the localized forms and includes l...
متن کاملOral Focal Mucinosis: A Rare Case Report of Two Cases
Oral focal mucinosis (OFM) is a rare soft tissue lesion of unknown etiology. Clinically, it is most commonly found on the gingiva and presents as a painless, sessile or pedunculated mass of the same colour as the surrounding mucosa. Histologically, it is characterized by focal myxoid degeneration of connective tissue. OFM occurs predominantly in adults during the fourth and fifth decade of life...
متن کامل[Papular mucinosis associated with hypothyroidism].
Papular mucinosis or lichen myxedematosus is an idiopathic disorder characterized by papules, nodules or plaques caused by mucin deposition in the dermis, in the absence of thyroid disease. The present report describes an atypical case with exuberant lesions in the form of plaques, associated with subclinical hypothyroidism. In cutaneous mucinosis, there is an abnormal quantity of mucin in the ...
متن کاملPapular atrichia: report of 3 cases with uncommon presentation
Atrichia with papular lesions (APL) is a rare, autosomal recessive syndrome with total alopecia in which mutations in the hairless gene have been shown to underlie the phenotype. We report here three cases, two 16 and 18 years old cousins and a 15 year-old-girl with a history of shedding of scalp, eyebrow and eye lashes in infancy. Later in life they developed numerous erythematous papules on t...
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ژورنال
عنوان ژورنال: TURKDERM
سال: 2018
ISSN: 1019-214X
DOI: 10.4274/turkderm.57689