Marta Stawczyk‐Macieja

ORCID: 0000-0001-8289-376X
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About
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Research Areas
  • Psoriasis: Treatment and Pathogenesis
  • Cancer and Skin Lesions
  • Dermatology and Skin Diseases
  • Autoimmune Bullous Skin Diseases
  • Nail Diseases and Treatments
  • Dupuytren's Contracture and Treatments
  • Skin Diseases and Diabetes
  • Medicine and Dermatology Studies History
  • Eosinophilic Disorders and Syndromes
  • Cutaneous lymphoproliferative disorders research
  • Oral health in cancer treatment
  • Skin and Cellular Biology Research
  • Inflammatory Myopathies and Dermatomyositis
  • Oral Health Pathology and Treatment
  • Genital Health and Disease
  • Histiocytic Disorders and Treatments
  • Plant Reproductive Biology
  • Vitamin D Research Studies
  • Vascular Malformations and Hemangiomas
  • Genetic and rare skin diseases.
  • Sarcoidosis and Beryllium Toxicity Research
  • Tattoo and Body Piercing Complications
  • Wnt/β-catenin signaling in development and cancer
  • Dermatological and Skeletal Disorders
  • Breast Lesions and Carcinomas

Gdańsk Medical University
2014-2021

Malignant acanthosis nigricans is a rare paraneoplastic skin syndrome mostly associated with gastric adenocarcinoma. Florid cutaneous papillomatosis and tripe palms are considered to be abortive clinical variants of nigricans. Clinical manifestations include pruritic, hyperkeratotic hyperpigmented plaques subsequent formation velvety papillomas in the involved areas. This case report describes an unusual patient diagnosed combination malignant nigricans, florid

10.5114/pdia.2014.40663 article EN Advances in Dermatology and Allergology 2014-01-01

Psoriasis genetic background depends on polygenic and multifactorial mode of inheritance. As in other complex disorders, the estimation disease risk based individual variants is impossible. For this reason, recent investigations have been focused combinations known psoriasis susceptibility markers order to improve evaluation. Our aim was compare score (GRS) for five loci involved immunological response (HLA-C, ERAP1, ZAP70) skin barrier function (LCE3, CSTA) between patients with chronic...

10.1371/journal.pone.0163185 article EN cc-by PLoS ONE 2016-09-22

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Błażewicz I, Szczerkowska-Dobosz A, Pęksa R, Stawczyk-Macieja M, Barańska-Rybak W, Nowicki R. Interstitial granulomatous dermatitis: a characteristic histological pattern with variable clinical manifestations. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii. 2015;32(6):475-477. doi:10.5114/pdia.2015.48060. APA Błażewicz, I., Szczerkowska-Dobosz, A., Pęksa, R., Stawczyk-Macieja, M.,...

10.5114/pdia.2015.48060 article EN cc-by-nc-sa Advances in Dermatology and Allergology 2015-01-01

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Stawczyk-Macieja M, Szczerkowska-Dobosz A, Rębała K, et al. ERAP1 and HLA-C*06 are strongly associated with the risk of psoriasis in population northern Poland. Advances Dermatology Allergology/Postępy Dermatologii i Alergologii. 2018;35(3):286-292. doi:10.5114/ada.2018.76226. APA Stawczyk-Macieja, M., Szczerkowska-Dobosz, A., Rębała, K., Gabig-Cimińska, Nowicki, R. J., & Haraś, A. (2018). Alergologii, 35(3),...

10.5114/ada.2018.76226 article PL Advances in Dermatology and Allergology 2018-01-01

Cutaneous T-cell lymphomas (CTCLs) are a diverse group of non-Hodgkin's with malignant T lymphocytes infiltrating the skin. Mycosis fungoides (MF) and Sézary syndrome (SS) belong to CTCLs, among others. In previous studies it was suggested that primary cancers more often occur in patients cutaneous lymphoma.To analyse incidence other malignancies CTCL patients.The evaluation coexistence neoplasms conducted by analysis patients' database, diagnosis mycosis syndrome, treated Dermatological...

10.5114/ada.2021.106205 article EN Advances in Dermatology and Allergology 2021-01-01

Epidermolysis bullosa is a group of inherited blistering skin diseases resulting in most cases from missense mutations KRT5 and KRT14 genes encoding the basal epidermal keratins 5 14. Here, we present patient diagnosed with localized subtype epidermolysis simplex caused by heterozygous mutation p.Ala428Asp gene, that has not been previously identified. Moreover, bioinformatic analysis novel was performed, showing changes interaction network between proteins. Identification genotype-phenotype...

10.1111/exd.13788 article EN Experimental Dermatology 2018-09-22

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Błażewicz I, Barańska-Rybak W, Stawczyk-Macieja M, Petranyuk A, Nowicki R. Plasma cell mucositis – a rare differential diagnosis for ulceration of oral mucosa. Dermatology Review/Przegląd Dermatologiczny. 2015;102(6):520-523. doi:10.5114/dr.2015.55699. APA Błażewicz, I., Barańska-Rybak, W., Stawczyk-Macieja, M., Petranyuk, A., & Nowicki, (2015). Dermatologiczny, 102(6), 520-523....

10.5114/dr.2015.55699 article IT cc-by-nc-sa Dermatology Review 2015-01-01

Confluent macular violaceous erythema on the anterior neck and chest in patients of dermatomyositis is called "V" sign (Fig. 1) [1,2]. VACCINOID SIGNA slight cutaneous reaction to vaccination a person partially immune small pox [3]. VAGABOND'S SIGN1. Parasitic melanoderma; discoloration skin persons filthy habits, caused by irritation lice [4].Also Greenhow's 2. A pigmentary process from an itching disease like prurigo pityriasis stimulating morbus Addisonii, particularly found vagrants...

10.7241/ourd.20193.34 article EN cc-by Our Dermatology Online 2019-07-01

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Stawczyk-Macieja M, Szczerkowska-Dobosz A, Jaśkiewicz-Nyckowska D. Dermatitis herpetiformis misdiagnosed and treated as tinea cutis glabrae. Dermatology Review/Przegląd Dermatologiczny. 2016;103(1):56-59. doi:10.5114/dr.2016.57745. APA Stawczyk-Macieja, M., Szczerkowska-Dobosz, A., & Jaśkiewicz-Nyckowska, (2016). Dermatologiczny, 103(1), 56-59. https://doi.org/10.5114/dr.2016.57745 Chicago Marta, Aneta Dorota...

10.5114/dr.2016.57745 article EN cc-by-nc-sa Dermatology Review 2016-01-01

AMA Jaśkiewicz-Nyckowska D, Szczerkowska-Dobosz A, Stawczyk-Macieja M, Czubek M. Severe hereditary punctate palmoplantar keratoderma (Brauer-Buschke-Fischer syndrome). Dermatology Review/Przegląd Dermatologiczny. 2015;102(3):233-236. doi:10.5114/dr.2015.51925. APA Jaśkiewicz-Nyckowska, D., Szczerkowska-Dobosz, A., Stawczyk-Macieja, M., & Czubek, (2015). Dermatologiczny, 102(3), 233-236. https://doi.org/10.5114/dr.2015.51925 Chicago Dorota, Aneta Marta and Maria Czubek. 2015. "Severe...

10.5114/dr.2015.51925 article EN cc-by-nc-sa Dermatology Review 2015-01-01

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Górska K, Szczerkowska-Dobosz A, Purzycka-Bohdan D, Stawczyk-Macieja M, Wierzba Nowicki RJ. Raynaud’s phenomenon as an interdisciplinary problem. Dermatology Review/Przegląd Dermatologiczny. 2017;104(5):499-508. doi:10.5114/dr.2017.71215. APA Górska, K., Szczerkowska-Dobosz, A., Purzycka-Bohdan, D., Stawczyk-Macieja, M., Wierzba, & Nowicki, R. J. (2017). Dermatologiczny, 104(5), 499-508....

10.5114/dr.2017.71215 article EN cc-by-nc-sa Dermatology Review 2017-01-01

Eponyms are used almost daily in the clinical practice of dermatology. And yet, information about person behind eponyms is difficult to find. Indeed, who is? What this person’s nationality? Is alive or dead? How can one find paper which first described disease? describe not only disease, but also signs, surgical procedures, staining techniques, pharmacological formulations, and even pieces equipment. In article we present symptoms starting with (V) other. The their synonyms, those have...

10.7241/ourd.20194.34 article EN cc-by Our Dermatology Online 2019-10-03
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