Eruptive collagenomas.
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A 24-year-old woman presented with hypopigmented papules of the abdomen that had been present for four years without a family history of similar cutaneous findings or associated medical problems. Histopathologic features confirmed the diagnosis of a connective-tissue nevus that was composed of collagen. Eruptive collagenomas are a rare form of acquired collagenomas, which are characterized by the sudden appearance of asymptomatic papules and nodules on the lower trunk and extremities; the lesions are composed of haphazardly arranged collagen fibers. The pathogenesis is unknown, lesions are persistent, and therapeutic options have not been reported. (+info)
Liver pathology in collagen vascular disorders highlighting the vascular changes within portal tracts.
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Pelvic organ prolapse and collagen-associated disorders.
(67/154)
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A review of the principles of radiological assessment of skeletal dysplasias.
(68/154)
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Folding delay and structural perturbations caused by type IV collagen natural interruptions and nearby Gly missense mutations.
(69/154)
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A canine autosomal recessive model of collagen type III glomerulopathy.
(70/154)
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Structural basis of fibrillar collagen trimerization and related genetic disorders.
(71/154)
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Serum biomarker analysis of collagen disease patients with acute-onset diffuse interstitial lung disease.
(72/154)
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