Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Intercellular deposition"'
Publikováno v:
The American Journal of Dermatopathology. 43:510-513
Cutaneous reactions surrounding abdominal stoma sites are typically irritant, allergic, infectious, traumatic or pathergic in etiology. Pemphigus, which encompasses a group of vesiculobullous autoimmune skin disorders, is seldom encountered as a peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40d7e4309c49af555bbdfd9a4e8f8053
https://doi.org/10.1097/dad.0000000000001845
https://doi.org/10.1097/dad.0000000000001845
Autor:
Manu V Harikumar, Reena Rai
Publikováno v:
Indian Dermatology Online Journal, Vol 8, Iss 5, Pp 319-322 (2017)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
Background: Pemphigus is a chronic autoimmune bullous disorder characterized by autoantibodies directed against desmoglein 3 and/or 1. Demonstration of intercellular deposition of IgG on the cell surface of keratinocytes by direct immunofluorescence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::408bc30d48b72e78a91096862636e984
http://www.idoj.in/article.asp?issn=2229-5178
http://www.idoj.in/article.asp?issn=2229-5178
Punctal and peri-punctal involvement in Urbach-Wiethe syndrome: case report and review of literature
Publikováno v:
Orbit. 38:474-476
Urbach-Weithe syndrome is an exceedingly rare multisystem disorder characterized by pathognomonic clinical findings of multiple beaded papules along the eyelid margins and peri-ocular areas and hoarseness of voice secondary to intercellular depositio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50775173fe4ac47ec2477b26d9788724
https://doi.org/10.1080/01676830.2018.1550791
https://doi.org/10.1080/01676830.2018.1550791
Autor:
Mitali Madhumita Rath, Pranita Mohanty
Publikováno v:
Journal of Dr. NTR University of Health Sciences, Vol 6, Iss 3, Pp 166-168 (2017)
Lipoid proteinosis or Urbach–Wiethe disease is a very rare autosomal recessive disease. The term was first coined by Urbach. This disorder is characterized by intercellular deposition of periodic-acid Schiff-positive amorphous hyaline material in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f32865d7dd58c8aaa6010fb638ba796b
http://www.jdrntruhs.org/article.asp?issn=2277-8632
http://www.jdrntruhs.org/article.asp?issn=2277-8632
Autor:
Christine J. Ko, Jennifer M. McNiff
Publikováno v:
Journal of Cutaneous Pathology. 41:293-296
Intercellular epidermal deposition of immunoglobulin G (IgG) in a continuous net-like or ‘chicken wire’ pattern is a well-described and diagnostic finding in direct immunofluorescence (DIF) studies of pemphigus. In our experience, punctate or dot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ea81c04f90d44d0409a9fb556fbed5a
https://doi.org/10.1111/cup.12272
https://doi.org/10.1111/cup.12272
Publikováno v:
Veterinary Dermatology. 3:79-84
— An 8 year old intact female German shepherd dog was presented with well demarcated symmetric facial erosions, ulcerations and crusting. Systemic illness was absent, and oral involvement occurred only late in the course of the disease. Skin biopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68dce03fe2cc0f94f0aae480f0e9517c
https://doi.org/10.1111/j.1365-3164.1992.tb00149.x
https://doi.org/10.1111/j.1365-3164.1992.tb00149.x
Publikováno v:
International journal of pediatric otorhinolaryngology. 68(12)
Lipoid proteinosis is a rare autosomal recessive disorder characterized by intercellular deposition of an amorphous hyaline material. It mainly involves skin and mucosal membranes of upper aerodigestive tract as well as central nervous system, lung,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6230d4b8bd348277ea8a6f100f0cf666
https://pubmed.ncbi.nlm.nih.gov/19758708
https://pubmed.ncbi.nlm.nih.gov/19758708
Autor:
Mariano Ara, F.J. Carapeto, Marta Lorda, Cristina Corredera, Ana Luisa Morales Moya, Victoria Fuentelsaz, Raquel Conejero, María Pilar Grasa
Publikováno v:
Journal of the American Academy of Dermatology. 66:e127-e128
From Lo Fund Conf Repr D A 56-year-old woman presented with a 3-month history of vegetating lesions that began as flaccid bullae. She denied systemic symptoms or ingestion of suspicious drugs. The physical examination revealed well demarcated, symmet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5300e4dfe8423758de966d8b96b07d0
https://doi.org/10.1016/j.jaad.2011.05.041
https://doi.org/10.1016/j.jaad.2011.05.041
Publikováno v:
Archives of Dermatology. 130:1454
In our 1989 article, we described a unique case characterized as lichen planus pemphigoides with features of lichen planus and pemphigus vulgaris. 1 This 76-year-old woman had a history of intra-abdominal lymphoma. A generalized blistering eruption d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b11e9af8830378ed59645a93df10d181
https://doi.org/10.1001/archderm.1994.01690110124030
https://doi.org/10.1001/archderm.1994.01690110124030
Autor:
Hiroshi Saito, Mutsuo Murata, Masanori Onishi, Yukihiro Hamaguchi, Yoshio Hirano, Yuichiro Yamamoto
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 32:193-202
Amyloidosis is a disease characterized by the intercellular deposition of amyloid fibrils in various tissues and organs. The eitology and treatment method are unknown in spite of many studies.A case of primary amyloidosis is reported. The patient was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1976c50bbbf5ccf7ea684da0b086cc83
https://doi.org/10.5794/jjoms.32.193
https://doi.org/10.5794/jjoms.32.193