Connective Tissue Nevi
Background:
Connective tissue nevi (CTN) are hamartomas in which components of the dermis (collagen, elastin, or glycosaminoglycans) are altered.
Appear as firm, asymptomatic, skin-colored plaques composed of closely grouped papules with an orange peel-like surface texture.
Previous classifications made based on which dermal component was found in excess, genetic patterns of inheritance, and +/- organ involvement fail to explain all reported cases. o Example: Buschke-Ollendorff syndrome (BOS), an autosomal dominant form characterized by juvenile elastomas a/w osteopoikilosis (multiple osteosclerotic bone lesions), where phenotypic expression varies.
Objective:
Characterize the clinical and histopathologic features of CTN and to highlight a spectrum of clinical disease.
Methods:
Retrospective study of cases selected based on strict clinical and histopathologic criteria. Patients identified by searching investigator’s clinical and histopathology files using key words. Total of 33 patients with CTN included in study, 31 children and two adults.
One pathologist performed all histopathologic analyses. o Specimens divided into 4 histopathologic groups: 1) “pure” collagenoma; 2) “pure elastoma”; 3) mixed type CTN with both collagen and elastic changes; 4) cellular CTN which an increased number of normal looking fibroblasts was observed + fiber changes.
Results:
Average age of onset at which the first signs were observed was 2 years. Three clinical forms were distinguished: o type A characterized by localized papules confined to one site, with one case presenting as an ulcerated infiltrated plaque o type B with two or more sites of involvement most often on thighs, lumbar region, thorax, abdomen, buttocks, arms, and legs o type C with unusually severe infiltration with functional impairment of a limb.
Histopathologic examination of lesional biopsy specimens showed 10 collagenomas, one elastoma, 18 mixed CTN, and an
Connective tissue nevi (CTN) are hamartomas in which components of the dermis (collagen, elastin, or glycosaminoglycans) are altered.
Appear as firm, asymptomatic, skin-colored plaques composed of closely grouped papules with an orange peel-like surface texture.
Previous classifications made based on which dermal component was found in excess, genetic patterns of inheritance, and +/- organ involvement fail to explain all reported cases. o Example: Buschke-Ollendorff syndrome (BOS), an autosomal dominant form characterized by juvenile elastomas a/w osteopoikilosis (multiple osteosclerotic bone lesions), where phenotypic expression varies.
Objective:
Characterize the clinical and histopathologic features of CTN and to highlight a spectrum of clinical disease.
Methods:
Retrospective study of cases selected based on strict clinical and histopathologic criteria. Patients identified by searching investigator’s clinical and histopathology files using key words. Total of 33 patients with CTN included in study, 31 children and two adults.
One pathologist performed all histopathologic analyses. o Specimens divided into 4 histopathologic groups: 1) “pure” collagenoma; 2) “pure elastoma”; 3) mixed type CTN with both collagen and elastic changes; 4) cellular CTN which an increased number of normal looking fibroblasts was observed + fiber changes.
Results:
Average age of onset at which the first signs were observed was 2 years. Three clinical forms were distinguished: o type A characterized by localized papules confined to one site, with one case presenting as an ulcerated infiltrated plaque o type B with two or more sites of involvement most often on thighs, lumbar region, thorax, abdomen, buttocks, arms, and legs o type C with unusually severe infiltration with functional impairment of a limb.
Histopathologic examination of lesional biopsy specimens showed 10 collagenomas, one elastoma, 18 mixed CTN, and an