ABSTRACT
Satoyoshi syndrome is a rare multisystemic disorder characterized by alopecia, diarrhea, muscle spasms, osseous abnormalities, and endocrinopathies. We report a case of Satoyoshi syndrome misdiagnosed as vitamin D-dependent rickets for several years.
Subject(s)
Alopecia/complications , Alopecia/etiology , Alopecia/pathology , Bone and Bones/abnormalities , Diarrhea/complications , Diarrhea/pathology , Spasm/complications , Spasm/pathology , Alopecia/diagnostic imaging , Bone and Bones/diagnostic imaging , Bone and Bones/pathology , Child , Diagnostic Errors , Diarrhea/diagnostic imaging , Female , Humans , Osteolysis/diagnostic imaging , Osteolysis/etiology , Radiography , Skin/pathology , Spasm/diagnostic imagingABSTRACT
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis mainly described in asian subjects. Here, we report a case of a caucasian 11-year-old boy with DUH and an unaffected twin brother. Parents were not consanguineous. A review of the main phenotical, clinical and hystological aspects of this rare entity is exhibited. Differential diagnose might be stablished with several pigmentary disorders, so Dermatologist might have this entity in mind to make a correct diagnose, specially in cases with no response to typical treatments.
Subject(s)
Outpatient Clinics, Hospital , Skin Diseases/epidemiology , Adult , Cross-Sectional Studies , Emergency Medical Services , Female , Humans , Keratosis, Seborrheic/diagnosis , Keratosis, Seborrheic/epidemiology , Keratosis, Seborrheic/therapy , Male , Skin Diseases/diagnosis , Skin Diseases/therapy , Spain/epidemiologySubject(s)
Anticholesteremic Agents/administration & dosage , Cholesterol/administration & dosage , Ichthyosis/drug therapy , Lovastatin/administration & dosage , Nevus/drug therapy , Sjogren-Larsson Syndrome/drug therapy , Skin Neoplasms/drug therapy , Adult , Drug Therapy, Combination , Female , Humans , Nevus/pathology , Sjogren-Larsson Syndrome/pathology , Skin Neoplasms/pathology , Young AdultABSTRACT
Mantle cell lymphoma is a type of non-Hodgkin lymphoma that affects extranodal areas, especially, bone narrow, digestive tract and Waldeyer ring. Here we report a case of mantle cell lymphoma IV Ann Arbor stage with cutaneous lesions on nasal dorsum and glans penis as the first manifestations. Skin involvement is a very rare manifestation and less than 20 cases have been reported in the literature. The importance of establishing multidisciplinary relationships for a global approach has been shown by this clinical case.
