An association of malignant eccrine poroma and venous insufficiency of lower extremity

Ekrin poroma nadir görülen ve ekrin ter bezlerinden kaynaklanan bir deri tümörüdür. Bu tip tümörler oldukça yavas büyürler ve diger deri kanserleriyle karısabilirler. Malign ekrin poroma ve venöz yetmezlik beraberligi literatürde simdiye kadar bildirilmemistir. Olgumuzda, sol bacak orta-arka kısmında variköz zeminde yerlesmis ekrin poroma kitlesi mevcuttu. Tanı histopatolojik degerlendirme ile konuldu. Lenf nodu ya da uzak organ metastazı saptanmadı. Bizler bu makalede 72 yasındaki bir bayan olguda, sol bacakta venöz yetmezlikle beraber görülen bir ekrin poroma kitlesinin basarılı cerrahi tedavisini sunmaya çalıstık. Bu birlikteligin tesadüfî olması veya venöz yetmezlik zemininde ekrin poroma gelismis olması olasılıgı aydınlatılamamıstır. Ancak bu makale ile bu çok nadir birliktelik tartısılmıstır.Eccrine poroma is a malignant tumour of eccrine sweat glands. It is a very rare, slow growing tumour and clinically resembles other skin cancers.We report a malignant eccrine poroma located on varicose surface of the posterior left leg of a 72 year-old woman. It was diagnosed by histopathological findings. Lymph nodes or distant metastases were not found. Malignant eccrine poroma with venous insufficiency has not been reported in the literature.Although we do not know how venous insufficiency effected the the development of eccrine poroma in our case we discuss this very rare association of eccrine poroma and venous insufficiency

Acquired unilateral nevoid telangiectasia syndrome accompanied by chronic hepatitis B virus infection

Letter to the editor doesn\u27t require summar

Boyunda lupus vulgaristen gelişen skuamoz hücreli karsinom

Lupus vulgaris (LV) is the most commonly encountered form of cutaneous tuberculosis, and the most common site of involvement is the head and neck. We report the case of a 45-year-old man with a squamous cell carcinoma arising from a plaque of LV with a 20-year history on the malar region and the neck. The patient presented with a 3-month history of a squamous cell carcinoma enlarging on the left neck. He has been successfully treated with tumor excision and antituberculous therapy. © 2011 Düzce Medical Journal

Lupus vulgaris: 30 years of experience from eastern Turkey

Atasoy, Mustafa/0000-0003-1904-9878WOS: 000269538800039PubMed: 19456796

Is prurutis trigger bandlike pattern Darier disease: Positive Koebner phenomenon?

Darier's disease is an uncommon autosomal dominant genodermatosis characterized by corrupted keratinisation of the epidermis, nails and mucous membranes. A 35-year-old female patient had papular lesions on axillary, inguinal and abdominal regions. The lesions on abdominal region appeared after pruritis. Histopathologic examination of the lesion was consistent with Darier's disease

A Case of Acrodermatitis Chronica Atrophicans Causedby Borrelia burgdorferi Infection

Lyme hastalığı Borrelia burgdorferi'nin neden olduğu multisistemik bir zoonozdur. B. burgdorferi Spirochaetacea ailesinden gevşek kıvrımlı ve hareketli bir spiroket olup, İxodes cinsi sert kenelerin ısırması ile insanlara geçmektedir. Eritema migrans, akrodermatitis kronika atrofikans ve morfea benzeri lezyonlar, deri bulguları olarak karşımıza çıkabilmektedir. Geç dönem lezyonu olan ve sıklıkla kırk yaş üstü kadınlarda görülen akrodermatitis kronika atrofikans, kızarıklık ve şişlikle başlayıp aylar ya da yıllar içinde atrofi ve skleroza neden olabilmektedir. Bu raporda akrodermatitis kronika atrofikansa neden olan bir B. burgdorferi enfeksiyonunun sunulması amaçlanmıştır.Lyme disease is a multisystemic zoonosis caused by Borrelia burgdorferi. B. burgdorferi is a motile spirochete with loose spirals from Spirochaetaceae family and Lyme disease is acquired by humans through the bite of hard ticks of Ixodes species. Erythema migrans, acrodermatitis chronica atrophicans and morphea-like lesions present as skin lesions. Acrodermatitis chronica atrophicans that is the late lesion of Lyme disease and that is often seen in women over the age of forty presents as hyperemia and swelling and can lead to atrophy and sclerosis within months or years. In this study we report a case of acrodermatitis chronica atrophicans caused by B. burgdorferi infection

Acute generalized exanthematous pustulosis associated with terbinafine: a case report

WOS: 000323527300010PubMed: 23432048A 27-year-old male patient who has used oral terbinafine for two weeks was admitted to our outpatient clinic for non-follicular millimetric pustules on erythematous and edematous different-sized plaques on his trunk and flexural areas. He was diagnosed with acute generalized exanthematous pustulosis (AGEP) because of terbinafine use in the light of history, clinical and histopathological findings. An AGEP is a rare and severe pustular reaction usually triggered by systemic drug intake. Approximately, 2.3% of the patients having oral terbinafine have been reported to develop cutaneous adverse effects. Although terbinafine is a commonly used medicine, it must be considered that it may cause severe adverse reactions

Diyabetli bir hastada primer kutanöz aktinomikoz

Actinomycosis is a chronic suppurative granulomatous infection caused by gram positive bacterium. Enfection especially affects the head, neck, thorax and abdomen. Primary cutaneous involvement is uncommon and has an association with trauma and local ischemia. We present one such case of primary cutaneous actinomycosis on the elbow of a 68 year old man with diabetes and external trauma. This patient was admitted to our clinic with a 10-12cm size blue-purple plaque. Skin biopsy revealed the characteristic 'sulphur granules' of actinomycosis in the deep dermis After the diagnosis, initially he was treated with penisilin and cotrimaxazol with a little effect. Treatment was continued with amoksisilin and cotrimaxazol and he respond to this medical treatment partially. After this medical therapy skin graft operation was performed. Lesions relapsed six months later. Medical therapy was repeated and still continues