Ali Tahsin Güneş
Dokuz Eylül University
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Featured researches published by Ali Tahsin Güneş.
International Journal of Dermatology | 2000
Sebnem Özkan; Neşe Atabey; Emel Fetil; Verda Erkizan; Ali Tahsin Güneş
Background Borrelia burgdorferi (Bb) infection has been implicated in the development of morphea and lichen sclerosus; however, conflicting results have been reported with different investigational methods from different regions. We looked for evidence of Bb in patients with morphea and lichen sclerosus by polymerase chain reaction (PCR) analysis of of skin biopsy samples.
Journal of The American Academy of Dermatology | 2000
Şebnem Özkan; Emel Fetil; Fatih İzler; Ugur Pabuccuoglu; Nagihan Yalçin; Ali Tahsin Güneş
Anetoderma is a rare disorder of cutaneous atrophy with loss of dermal elastic tissue. Secondary anetoderma is seen after a variety of dermatoses. We describe a 33-year-old woman with secondary anetoderma after generalized granuloma annulare lesions that were most pronounced on sun-exposed areas.
Journal of Dermatology | 2004
Mustafa Turhan Şahin; Serap Öztürkcan; Aylin Türel Ermertcan; Ali Tahsin Güneş
Clinical differentiation of facial lentigo senilis/initial seborrheic keratosis (LS/ISK), seborrheic keratosis (SK), lentigo maligna (LM), and lentigo maligna melanoma (LMM) can be difficult. Dermoscopy improves the diagnoses in pigmented skin lesions (PSLs), but it is not helpful for the sun‐exposed face because of the flat rete ridges without network‐derived features. Therefore, development of new diagnostic criteria for this particular localization is a current issue of dermatology. In this retrospective study, dermoscopic slides of facial pigmented skin lesions of 66 patients referred to two clinics in Turkey were evaluated. Our aim was to determine the reliability of dermoscopy in the differentiation of these entities. The facial PSLs of 66 patients (34 males and 32 females) (median age: 58.2) were photographed with a Dermaphot (Heine, Hersching, Germany) over a five year period from November of 1995 to May of 2000. All of the dermoscopic slides were analysed according to 27 dermoscopic criteria developed by Schiffner et al. This data set contained 22 histologically proven malignant (14 LM, 8 early LMM) and 44 benign (18 SK, 26 LS/ISK) PSLs. In general, asymmetric pigmented follicular openings, dark streaks, slate‐gray streaks, dark globules, slate‐gray globules, dark dots, dark rhomboidal structures, light brown rhomboidal structures, dark homogeneous areas and dark pseudonetworks were statistically significant for malignant growth. On the other hand, milia‐like cysts, pseudofollicular openings, cerebriform structures, light brown globules, light brown dots, light brown homogeneous areas, yellow opaque homogeneous areas, and light brown pseudonetworks were statistically significant for benign growth. This research emphasizes that dermoscopic features on the face differ from criteria used in other locations of the body. Analysis of the data suggests that dermoscopy can be used in the differentiation of LS/ISK, SK, LM and LMM from each other.
Journal of The European Academy of Dermatology and Venereology | 2011
L Babayeva; Sevgi Akarsu; Emel Fetil; Ali Tahsin Güneş
Background No single effective topical treatment is available for treating all pathogenic factors causing acne vulgaris (AV). Salicylic acid (SA), tretinoin (all‐TRA) and clindamycin phosphate (CDP) are known to to be effective agents depending on their comedolytic and anti‐inflammatory properties.
Journal of Dermatology | 2006
Turna Ilknur; Emel Fetil; Sevgi Akarsu; Didem Didar Altiner; Cagnur Ulukus; Ali Tahsin Güneş
Angioma serpiginosum is a rare benign vascular disorder, characterized clinically by multiple minute, red to purple, grouped macules in serpiginous and gyrate patterns and histopathologically by ectatic dilatation of capillaries. Patients can undergo unnecessary hematological tests, because the condition can be confused with chronic purpuric dermatoses. An 18‐year‐old man with angioma serpiginosum of his left arm was evaluated by dermoscopy and treated with pulsed dye laser. Numerous small, relatively well‐demarcated, round to oval red lagoons were determined with dermoscopy, and approximately 75% of the area of his lesion disappeared after four sessions of pulsed dye laser. Our case supports the hypothesis that dermoscopy is beneficial in the diagnosis of angioma serpiginosum and that pulsed dye laser is effective in the treatment of this disorder.
Clinical and Experimental Dermatology | 2007
Ali Tahsin Güneş; Turna Ilknur; Ugur Pabuccuoglu; Banu Lebe; Didem Didar Altiner
Acantholytic dyskeratosis is a distinct histological pattern characterized by hyperkeratotic and parakeratotic epidermis with intraepidermal clefts harbouring acantholytic and dyskeratotic keratinocytes. This histopathological pattern is uncommon in dermatoses of the anogenital region. We report a 30‐year‐old woman who had numerous smooth whitish papules on the labia majora, perineum and perianal region, which coalesced into plaques in some areas. Microscopically, the lesions showed prominent suprabasal and intraspinous acantholysis with dyskeratotic keratinocytes. Direct immunofluorescence examination revealed intercellular Ig G and C3 within the epidermis. We were unable to find a similar case of papular acantholytic dyskeratosis of the anogenital area with positive direct immunofluorescence findings reported in the literature, thus in this report, the clinicopathological features of a unique case are presented.
International Journal of Dermatology | 2006
Ali Tahsin Güneş; Emel Fetil; Turna Ilknur; Bahar Birgin; Sebnem Özkan
Background Clinical and histopathological differential diagnosis is usually impossible in drug‐induced lichen planus (LP) and idiopathic LP. Naproxen is a nonsteroidal anti‐inflammatory drug, which is widely used for its analgesic, antipyretic and anti‐inflammatory effects. To the best of our knowledge, two case reports on naproxen‐induced LP have been reported.
International Journal of Dermatology | 2002
Emel Fetil; Sebnem Özkan; Turna Ilknur; Yasemin Erdem; Banu Lebe; Ali Tahsin Güneş
A 22‐year‐old woman presented to our clinic with a complaint of masses on various parts of her body. A mass on her right forearm had appeared 5 years ago and had enlarged during the past 6 months. Two lesions on the back of her neck had a 3‐year history, one lesion on her eyebrow had a 2‐year history, and one lesion on her left forearm had a 1‐year history. The lesion on her left forearm was discharging purulent material.
Photodermatology, Photoimmunology and Photomedicine | 2006
Emel Fetil; Sevgi Akarsu; Turna Ilknur; Ergun Kusku; Ali Tahsin Güneş
Background/purpose: Various topical agents which can be used in combination with phototherapy may have blocking or enhancing effects. In this in vivo study, the effects of topical petrolatum, basis cream, glycerine and olive oil on the transmission of ultraviolet B (UVB) were investigated.
Dermatology | 2002
Emel Fetil; Sebnem Özkan; Nalan Gürler; Ergun Kusku; Füsun Arda; Ali Tahsin Güneş
The Leser-Trélat (LT) sign refers to the sudden appearance of numerous seborrheic keratoses (SK) or the sudden increase in the number and the size of SK in association with an internal malignancy [1–3]. The existence of the LT sign has been explored for many years; its validity is still a point of controversy [2–6]. We report a patient with the sudden appearance of multiple SK along with a visceral malignancy and within several years a second visceral malignancy occurring along with a sudden increase in the size and number of her SK. A 66-year-old woman was admitted to our clinic with a complaint of several skin lesions occurring on her trunk. She had noticed their development rapidly in the previous 6–7 months. They were associated with mild pruritus. Her medical history included diabetes mellitus, hypertension and mitral and aortic valve insufficiency. Physical examination revealed multiple disseminated sharply demarcated, round or oval verrucous, tan or light brown papules with follicular plugs of 3–10 mm in size on the chest, abdomen and back (fig. 1). They were diagnosed as SK clinically and histopathologically.