منابع مشابه
Prurigo pigmentosa: an underdiagnosed disease?
Prurigo pigmentosa is a distinctive inflammatory disease first described by the Japanese dermatologist Masaji Nagashima in 1971. It is typified by recurrent, pruritic erythematous macules, papules and papulovesicles that resolve leaving behind netlike pigmentation. The disease is rarely diagnosed outside Japan, because clinicians outside Japan are not well conversant with the criteria for its d...
متن کاملActinic Prurigo: A case report
Actinic prurigo is a rare disease occurring mainly in individuals of American Indian origin and those living in high altitudes. Skin lesions consist of pruritic popular or nodular excoriated lesions mainly affecting exposed skin but covered skin is also involved in up to 50% of patients. This is the first case report of an Iranian patient. This 19-year-old female had pruritic popular and ...
متن کاملNodular Prurigo Associated with Mycosis Fungoides - Case Report.
Mycosis fungoides (MF) is the most common type of cutaneous lymphoma and accounts for approximately 50% of all lymphomas arising primarily in the skin. The three types of MF lesions are patches, plaques, and tumors, according to which the disease is traditionally divided into three clinical stages. The clinical course can be protracted and take years or decades. In the final stage, MF evolves t...
متن کاملRisk factors associated with actinic prurigo: a case control study*
BACKGROUND Actinic prurigo (AP) is an idiopathic photodermatosis. Although its initial manifestations can appear in 6 to 8-year-old children, cases are diagnosed later, between the second and fourth decades of life, when the injuries are exacerbated. OBJECTIVE To identify risk factors associated with clinical manifestations of AP such as skin and mucosal lesions. METHODS Thirty patients wit...
متن کاملMotor neuron disease and its association with non-Hodgkins lymphoma.
M otor neuron disease (MND) is a neurodegenerative disorder characterized by muscle atrophy, brisk reflexes, spasticity, fasciculation, and atrophy. The onset of the disease is generally insidious. The pathological process may involve the motor cortex, the spinal cord, and the brainstem. 1 Only upper or only lower motor neurons may be affected. The disease may or may not be seen with neoplasms,...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1918
ISSN: 0035-9157
DOI: 10.1177/003591571801100257