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Lewandowsky and lutz dysplasia: report of two cases in a family.

Bhutoria B, Shome K, Ghosh S, Bose K, Datta C, Bhattacharya S - Indian J Dermatol (2011)

Bottom Line: Differential clinical and histopathologic evolutions of lesions in two cases of familial EV are compared and discussed in detail.Cases were followed up for 7 years.This study reveals that the disease progression is variable among two individuals of the same family.

View Article: PubMed Central - PubMed

Affiliation: Department of Pathology, Burdwan Medical College, Burdwan, West Bengal, India.

ABSTRACT
Lewandowsky and Lutz dysplasia, also known as epidermodysplasia verruciformis (EV), is an inherited disorder in which there is widespread and persistent infection with human papilloma virus, defect in cell-mediated immunity and propensity for malignant transformation. Differential clinical and histopathologic evolutions of lesions in two cases of familial EV are compared and discussed in detail. Cases were followed up for 7 years. Detailed history, clinical features and investigations, including skin biopsy from different sites at different times, were examined. Generalized pityriasis versicolor like hypopigmented lesions in both the cases, together with variable pigmented nodular actinic keratosis like lesions on sun-exposed areas, were present. Multiple skin biopsies done from various sites on different occasions revealed features typical of EV along with lesions, i.e., actinic keratosis, Bowen's disease, basal and squamous cell carcinoma, in the elder sibling. However, skin biopsy of the other sibling showed features of EV and seborrheic keratosis only till date. This study reveals that the disease progression is variable among two individuals of the same family. Malignant lesions were seen only on sun-exposed areas and may be associated with other skin lesions or infections such as angiokeratoma of Fordyce and tinea cruris, as seen in this report.

No MeSH data available.


Related in: MedlinePlus

Photograph of elder sibling showing angiokeratoma of Fordyce with EV
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Figure 5: Photograph of elder sibling showing angiokeratoma of Fordyce with EV

Mentions: Subsequently, 3 years later, the elder brother again presented to the department. On examination, the plaques had increased in number and were more confluent. In addition, there were hyperpigmented, black colored plaques over chest, back, abdomen, nose, right nasolabial fold and right cheek. Over the right scrotum, multiple angiomatous papules arranged in a linear pattern, suggestive of angiokeratoma of Fordyce were seen [Figure 5]. Also present were circinate patches over the groin.


Lewandowsky and lutz dysplasia: report of two cases in a family.

Bhutoria B, Shome K, Ghosh S, Bose K, Datta C, Bhattacharya S - Indian J Dermatol (2011)

Photograph of elder sibling showing angiokeratoma of Fordyce with EV
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3108519&req=5

Figure 5: Photograph of elder sibling showing angiokeratoma of Fordyce with EV
Mentions: Subsequently, 3 years later, the elder brother again presented to the department. On examination, the plaques had increased in number and were more confluent. In addition, there were hyperpigmented, black colored plaques over chest, back, abdomen, nose, right nasolabial fold and right cheek. Over the right scrotum, multiple angiomatous papules arranged in a linear pattern, suggestive of angiokeratoma of Fordyce were seen [Figure 5]. Also present were circinate patches over the groin.

Bottom Line: Differential clinical and histopathologic evolutions of lesions in two cases of familial EV are compared and discussed in detail.Cases were followed up for 7 years.This study reveals that the disease progression is variable among two individuals of the same family.

View Article: PubMed Central - PubMed

Affiliation: Department of Pathology, Burdwan Medical College, Burdwan, West Bengal, India.

ABSTRACT
Lewandowsky and Lutz dysplasia, also known as epidermodysplasia verruciformis (EV), is an inherited disorder in which there is widespread and persistent infection with human papilloma virus, defect in cell-mediated immunity and propensity for malignant transformation. Differential clinical and histopathologic evolutions of lesions in two cases of familial EV are compared and discussed in detail. Cases were followed up for 7 years. Detailed history, clinical features and investigations, including skin biopsy from different sites at different times, were examined. Generalized pityriasis versicolor like hypopigmented lesions in both the cases, together with variable pigmented nodular actinic keratosis like lesions on sun-exposed areas, were present. Multiple skin biopsies done from various sites on different occasions revealed features typical of EV along with lesions, i.e., actinic keratosis, Bowen's disease, basal and squamous cell carcinoma, in the elder sibling. However, skin biopsy of the other sibling showed features of EV and seborrheic keratosis only till date. This study reveals that the disease progression is variable among two individuals of the same family. Malignant lesions were seen only on sun-exposed areas and may be associated with other skin lesions or infections such as angiokeratoma of Fordyce and tinea cruris, as seen in this report.

No MeSH data available.


Related in: MedlinePlus