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    Atypical familial Papillon-Lefevre syndrome
    (European Acad Dermatology & Venereology, 2001) Inalöz, HS; Harman, M; Akdeniz, S; Inalöz, SS; Isik, AG
    The Papillon-Lefevre syndrome is a rare autosomal recessive disorder. Consanguinity seems a notable prerequisite. Papillon-Lefevre syndrome manifests in the first 6 months of life with rapidly progressive periodontitis and severe alveolar bone destruction leading to early loss of both the deciduous and permanent teeth in association with palmo-plantar hyperkeratosis. We present two unusual cases of familial Papillon-Lefevre syndrome, one of whom has only late onset of mild skin lesions and the other has severe skin lesions and relatively mild periodontal disease. A number of other cases recently described have also had atypical features.
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    Coexistence of psoriasis vulgaris and bullous disorders
    (Wiley, 1999) Aytekin, S; Inalöz, HS; Harman, M; Akdeniz, S; Deveci, E; Inalöz, SS
    [Abstract Not Available]
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    Congenital non-familial unilateral basaloid follicular hamartoma
    (Wiley, 1999) Harman, M; Inalöz, HS; Akdeniz, S; Inalöz, SS; Aslan, A
    Basaloid follicular hamartoma is not a well-recognized clinical entity and has often been diagnosed as trichoepithelioma or basal cell carcinoma. It is a unique benign follicular tumour which comprises a variety of clinical manifestations. We present the case of a 24-year-old male with unilateral basaloid follicular hamartoma present at birth and later misdiagnosed as basal cell carcinoma. Histological features of basaloid follicular hamartoma are nor always diagnostic and clinico-pathological correlation is particularly important to distinguish this benign hamartoma from other basaloid tumours including basal cell carcinoma. Continuous follow-up of our patient did not reveal any clinical or histological malignant transformation. (C) 1999 Elsevier Science B.V. All rights reserved.