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The Verhoeff stain, also known as the Verhoeff-van Gieson stain, is a histological staining procedure developed by Frederick Herman Verhoeff in 1908. The Verhoeff stain is one of the most commonly-used stains to visualize elastic tissue, as found in blood vessel walls, elastic cartilage, lungs, skin, bladder, and some ligaments.

Many disorders are known to have detrimental effects on both visceral and cutaneous elastic tissue. Marfan syndrome, caused by autosomal dominant mutations in the fibrillin-1 gene (FBN1), results in a defective scaffold for elastin deposition. Stains of aortic and cutaneous tissue samples from animal models of Marfan syndrome demonstrated decreased density and increased fragmentation of elastic lamellae and fibers, with tangled microfibrils. [8], [9], [10], [11] These abnormalities predispose Marfan patients to joint hypermobility and thoracic aorta aneurysms and dissections. Pseudoxanthoma elasticum (PXE), also known as Grönblad-Strandberg syndrome, is a progressive, genodermatosis typically inherited in an autosomal recessive manner. Mutations in the ATP-binding cassette subfamily C member 6 (ABCC6) gene result in ectopic calcification of elastic fibers in connective tissue throughout the body. [12] Manifestations of PXE include yellow papules along flexural surfaces, cutaneous laxity, retinal complications, premature atherosclerosis and valvular cardiac sequelae. Diagnosis of PXE is best accomplished through skin biopsy displaying elastorrhexis, characterized by fragmentation and mineralization of elastic fibers within the mid-reticular dermis on Verhoeff stain or stains for calcium. [13] Additionally, cardiac biopsy specimens from patients with PXE stained with the Verhoeff stain demonstrate coarse, curled, fragmented, disorganized and palisaded elastic fibers with substantial degeneration within the endocardium. [14]

Pseudoxanthoma elasticum (PXE), also known as Grönblad-Strandberg syndrome, is a progressive, genodermatosis typically inherited in an autosomal recessive manner. Mutations in the ATP-binding cassette subfamily C member 6 (ABCC6) gene result in ectopic calcification of elastic fibers in connective tissue throughout the body. [12] Manifestations of PXE include yellow papules along flexural surfaces, cutaneous laxity, retinal complications, premature atherosclerosis and valvular cardiac sequelae. Diagnosis of PXE is best accomplished through skin biopsy displaying elastorrhexis, characterized by fragmentation and mineralization of elastic fibers within the mid-reticular dermis on Verhoeff stain or stains for calcium. [13] Additionally, cardiac biopsy specimens from patients with PXE stained with the Verhoeff stain demonstrate coarse, curled, fragmented, disorganized and palisaded elastic fibers with substantial degeneration within the endocardium. [14] Verhoeff’s stain has also been used in the visualization of elastic fibers within elastofibromas. Elastofibromas are rare, ill-defined tumor-like growths composed of irregular and enlarged elastic fibers. They present as a firm, deep, rubbery, slow-growing mass, with a characteristic periscapular location deep to the skeletal musculature. [15], [16] Elastofibromas may be bilateral, although are uncommonly painful. The etiology of elastofibromas is unclear but may be secondary to an inherited predisposition, enzymatic defect causing abnormal elastic fiber formation or repeated friction. Microscopic evaluation reveals dense bands of collagen fibers, adipose tissue, and abnormal elastic fibers. [17] As viewed following Verhoeff stain, the elastic fibers are coarse, thick and globular, resulting in a beaded or “string-of-pearls” appearance with a serrated edge. [17], [18], [19]

Verhoeff’s stain has also been used in the visualization of elastic fibers within elastofibromas. Elastofibromas are rare, ill-defined tumor-like growths composed of irregular and enlarged elastic fibers. They present as a firm, deep, rubbery, slow-growing mass, with a characteristic periscapular location deep to the skeletal musculature. [15], [16] Elastofibromas may be bilateral, although are uncommonly painful. The etiology of elastofibromas is unclear but may be secondary to an inherited predisposition, enzymatic defect causing abnormal elastic fiber formation or repeated friction. Microscopic evaluation reveals dense bands of collagen fibers, adipose tissue, and abnormal elastic fibers. [17] As viewed following Verhoeff stain, the elastic fibers are coarse, thick and globular, resulting in a beaded or “string-of-pearls” appearance with a serrated edge. [17], [18], [19] The Verhoeff stain is particularly useful in the evaluation of pathologies of the elastic lamina found within elastic arteries, such as the aorta. The degenerative changes of the valvular leaflets seen in senile aortic stenosis may be visualized, in part, using the Verhoeff stain. One defining characteristic of early stenotic lesions is aortic-side subendothelial thickening with displacement and fragmentation of the internal elastic lamina, visualized on Verhoeff staining. [20], [21] Arteriosclerosis may appear as atrophy and fragmentation of elastin fibers within the lamina. [22], [23] Potential pathogenic mechanisms include lipid deposition, intimal fibrosis and increased local concentrations of elastases within the arterial elastic tissue. [23], [24], [22] The Verhoeff stain has also been commonly utilized in dermatopathology. Normal hair follicles are typically embedded within a sheath of elastic fibers. Histological alterations of the presence and distribution of follicular elastin can be used to differentiate various forms of alopecia, particularly those with a scarring or fibrosing etiology. [25], [26], [27]

The Verhoeff stain has also been commonly utilized in dermatopathology. Normal hair follicles are typically embedded within a sheath of elastic fibers. Histological alterations of the presence and distribution of follicular elastin can be used to differentiate various forms of alopecia, particularly those with a scarring or fibrosing etiology. [25], [26], [27] Unique distributions of elastic fibers can be identified by Verhoeff staining of several cutaneous neoplasms and similar lesions. [2] In melanoma, there is a lack of elastic fibers between malignant melanocytes; the elastic fibers appear forced downwards and crushed at the base of the tumor. [28], [29] In a case of melanoma arising within a nevus, elastic fibers may be noted to be absent from the melanoma component and retained within the nevus aspect of the lesion. [2] Melanocytic nevi present with elastic fibers dispersed throughout the benign melanocytes and in the papillary dermis, are oriented perpendicularly to the epidermis and have a forked appearance. [28] In keratoacanthomas, elastic fibers are limited to the basal aspects of the lesion (“elastic trapping”), differentiating them from hypertrophic lichen planus and squamous cell carcinoma. [30] In dermatofibromas, thickened and fragmented elastic fibers are arranged in parallel within the reticular dermis, sparing the pilosebaceous units. Scars typically demonstrate many fine elastic fibers on electron microscopy, although these are not well-identified by Verhoeff stains. [27], [31] Scars appear anelastotic on light microscopy until at least three months following the inciting trauma, although elastic fibers may be apparent on electron microscopy. [27], [31], [32] This discrepancy may be explained by the inability of the Verhoeff stain to identify thin, newly-formed elastic fibers. Hereditary and acquired disorders of cutaneous elastic tissue are commonly initially evaluated by skin biopsy, for which the Verhoeff-van Gieson stain may be utilized to visualize elastic fibers. Disorders of increased elastic tissue include focal elastosis and elastomas, while disorders of diminished elastic fibers include anetoderma, nevus anelasticus, cutis laxa and perifollicular elastolysis, among others. [33] Additionally, structural abnormalities of elastin fibers can be observed in cutis laxa and penicillamine-induced elastosis perforans serpiginosa. [34], [2]