A5080262673- Autoimmune Bullous Skin Diseases
- Urticaria and Related Conditions
- Dermatological and Skeletal Disorders
- Drug-Induced Adverse Reactions
- Vascular Malformations and Hemangiomas
- RNA Research and Splicing
- Dermatological and COVID-19 studies
- Muscle metabolism and nutrition
- Cardiac tumors and thrombi
- Cancer and Skin Lesions
- Inflammatory Myopathies and Dermatomyositis
- Eosinophilic Disorders and Syndromes
- COVID-19 and healthcare impacts
- melanin and skin pigmentation
- Skin and Cellular Biology Research
- Neonatal Health and Biochemistry
- Systemic Lupus Erythematosus Research
- Oral and Maxillofacial Pathology
- Contact Dermatitis and Allergies
- Vascular Tumors and Angiosarcomas
- Nuclear Structure and Function
- Psoriasis: Treatment and Pathogenesis
- Parvovirus B19 Infection Studies
- Herpesvirus Infections and Treatments
- Hemoglobinopathies and Related Disorders
Medical University of Sofia
2013-2022
Alexandrovska Hospital
2014
Abstract Although toxoplasmosis is one of the most widely spread infections in world, types that involve skin are extremely rare. However, lesions not specific; moreover, they quite diverse, which makes diagnosis cutaneous rather difficult. Thus, differential should include a number other diseases. We present case 43-year-old immunocompetent man with multiple livid erythematous papules and nodules yellowish discharge involved body extremities. By using electro-chemiluminescence immunoassay,...
Abstract Lupus erythematosus is an autoimmune connective tissue disorder showing a broad spectrum of clinical manifestations. The aim this study was to assess the correlation skin histology and different types lupus erythematosus. Materials methods: Fifty-one specimens were assessed from 39 female 12 male patients with acute, subcutaneous chronic erythematosus, diagnosed treated in Department Dermatology Venereology, Alexandrovska University Hospital for 4-year period. Results: Follicular...
No Data Availability Statement is present regarding the Letter.
Abstract Leucinosis (maple syrup urine disease - MSUD) is an inherited aminoacidopathy and organic aciduria caused by severe enzyme defect in the metabolic pathway of amino acids: leucine, isoleucine, valine. The classical variant characterized accumulation both α-keto acids, particulary most toxic rapid elevation circulating leucine its ketoacid, α-ketoisocaproate, which cause encephalopathy life-threatening brain swelling. However, patients with form, maple disease, may appear normal at...
Abstract Congenital generalized lipodystrophy (CGL), also known as Berardinelli-Seip syndrome (BSS), is a rare autosomal recessive disease characterized by near total absence of adipose tissue and muscular hypertrophy. Additional common clinical signs are acanthosis nigricans, acromegaloid features, hepatomegaly, hyperandrogenism, altered glucose intolerance, cardiomyopathy hypertriglyceridemia. An 11-year-old girl was admitted to our Clinic presenting with hyperandrogenic lack tissue,...
Lymphangiosarcoma is an uncommon vascular tumor that usually develops in chronic lymphedema. The etiology of lymphangiosarcoma remains unknown. It mainly after mastectomy, association with lymphedema (Stewart-Treves syndrome), or radiotherapy. early diagnosis this aggressive important, as it has a high risk local recurrence and metastasis. Stewart-Treves syndrome occurs 0.5% patients who survive mastectomy for more than 5 years. mean age at appearance the angiosarcoma 62 years, interval...
Ichthyosis hystrix is a term used to describe an autosomal dominant rare form of ichthyosiform dermatosis which characterized by hyperkeratotic spiny scales. We present healthy 22-year-old man with lesions clinically and histopathologically corresponded the inherited disorder ichthyosis hystrix.
Introduction: Generalized eruptive syringomas is a rare clinical presentation of benign adnexal tumor derived from the intraepidermal portion eccrine sweat ducts. Clinical shows asymptomatic flesh-colored tumors on anterior aspect trunk. Material and Methods : A case 51-year-old male with long-standing generalized eruption multiple brown-colored papules, associated odorous perspiration total loss teeth which appeared suddenly three years ago. Results: Punch biopsy specimen revealed normal...
Papillomatosis papulosa confluens reticulata et pigmentata is a rare dermatosis that presents clinically with pigmented, papillomatous, hyperkeratotic plaques central confluence and reticulated peripheral pattern. The etiology remains unclear but current data points to keratinization defect as the main pathological mechanism. There one case report in literature of UV-induced pigmentata. We present 16-year old patient clinical histological diagnosis confluent papillomatosis. characteristic...