Database : MEDLINE
Search on : Mucinoses [Words]
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[PMID]: 29460897
[Au] Autor:Radenska-Lopovok SG; Volkova P
[Ad] Address:I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
[Ti] Title:Skleromiksedema - dermatologicheskaia problema ili sistemnyi patologicheskii protsess? [Is scleromyxedema a skin problem or systemic pathological process?]
[So] Source:Arkh Patol;80(1):63-66, 2018.
[Is] ISSN:0004-1955
[Cp] Country of publication:Russia (Federation)
[La] Language:rus
[Ab] Abstract:Scleromyxedema is regarded as a rare cutaneous mucinosis from a group of lichen myxedematosus characterized by diffuse mucin deposition, sclerosis, and lichenoid eruptions in the absence of thyroid disease. The paper discusses the pathogenesis of the disease and histological changes in tissues. It underlines the need for using histochemical tests to identify acidic and neutral glycosaminoglycans and gives a differential diagnosis of this disease.
[Pt] Publication type:ENGLISH ABSTRACT; JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180220
[Lr] Last revision date:180220
[St] Status:In-Data-Review
[do] DOI:10.17116/patol201880163-66

  2 / 593 MEDLINE  
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[PMID]: 29245213
[Au] Autor:Wang N; Shan X; Wu W; Shen X; Hu TX; Pei Z; Wang K
[Ad] Address:aQilu Hospital of Shandong University, JinanbShandong Provincial Institute of Dermatology and Venereology, Jinan, ShandongcFirst Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, P. R. ChinadHarvard Medical School, Harvard University, Boston, Massachusetts, USA.
[Ti] Title:A case report of atypical nodular cutaneous lupus mucinosis.
[So] Source:Medicine (Baltimore);96(49):e8391, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:RATIONAL: Nodular cutaneous lupus mucinosis is regarded as a distinctive cutaneous mucinosis deposition with systemic lupus erythematosus(SLE). All typical cases occurred as asymptomatic cutaneous papules, nodules, or plaques on the trunk, upper and lower extremities, and face. Histopathology is mainly revealed abundant mucin deposits among splayed collagen bundles in the dermis. At the same time we can find A the typical clinical manifestations and biological evidence of SLE. Here, we report the first case of nodular cutaneous lupus mucinosis that did not present with any prior symptoms or history of SLE. PATIENT CONCERNS: We report the first case of nodular cutaneous lupus mucinosis that did not present with any prior symptoms or history of SLE. The patient was 34 years old. One year before admission, nodules began to appear on the elbows, chest, and back, and 2 months before admission erythema occurred on the face. Other notable clinical symptoms were not observed and had no prior history of SLE. DIAGNOSES: Initially, this patient was misdiagnosed by other clinics as having eczema. After histopathological assessment of skin biopsy and examination of antinuclear antibody signals, the patient was correctly diagnosed with nodular cutaneous lupus mucinosis. INTERVENTIONS: Followed administration of systemic steroids and hydroxychloroquine. OUTCOMES: the eruptions quickly disappeared and laboratory indicators improved. LESSONS: This case highlights the need for diagnostic vigilance in cases involving papules and nodules initially developing on the chest and elbows in the absence of obvious lupoid symptoms. We recommend a lower threshold for performing histopathological analysis and examination of antinuclear antibody signals in view of the rare but serious possibility of nodular cutaneous lupus mucinosis.
[Mh] MeSH terms primary: Lupus Erythematosus, Cutaneous/complications
Mucinoses/etiology
[Mh] MeSH terms secundary: Adult
Humans
Male
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171222
[Lr] Last revision date:171222
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:171217
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008391

  3 / 593 MEDLINE  
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[PMID]: 28712039
[Au] Autor:Ferreli C; Gasparini G; Parodi A; Cozzani E; Rongioletti F; Atzori L
[Ad] Address:Section of Dermatology, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy. ferreli@unica.it.
[Ti] Title:Cutaneous Manifestations of Scleroderma and Scleroderma-Like Disorders: a Comprehensive Review.
[So] Source:Clin Rev Allergy Immunol;53(3):306-336, 2017 Dec.
[Is] ISSN:1559-0267
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Scleroderma refers to an autoimmune connective tissue fibrosing disease, including three different subsets: localized scleroderma, limited cutaneous systemic sclerosis, and diffuse cutaneous systemic sclerosis with divergent patterns of organ involvement, autoantibody profiles, management, and prognostic implications. Although systemic sclerosis is considered the disease prototype that causes cutaneous sclerosis, there are many other conditions that can mimic and be confused with SSc. They can be classified into immune-mediated/inflammatory, immune-mediated/inflammatory with abnormal deposit (mucinoses), genetic, drug-induced and toxic, metabolic, panniculitis/vascular, and (para)neoplastic disorders according to clinico-pathological and pathogenetic correlations. This article reviews the clinical presentation with emphasis on cutaneous disease, etiopathogenesis, diagnosis, and treatment options available for the different forms of scleroderma firstly and for scleroderma-like disorders, including scleromyxedema, scleredema, nephrogenic systemic fibrosis, eosinophilic fasciitis, chronic graft-versus-host disease, porphyria cutanea tarda, diabetic stiff-hand syndrome (diabetic cheiroartropathy), and other minor forms. This latter group of conditions, termed also scleroderma mimics, sclerodermiform diseases, or pseudosclerodermas, shares the common thread of skin thickening but presents with distinct cutaneous manifestations, skin histology, and systemic implications or disease associations, differentiating each entity from the others and from scleroderma. The lack of Raynaud's phenomenon, capillaroscopic abnormalities, or scleroderma-specific autoantibodies is also important diagnostic clues. As cutaneous involvement is the earliest, most frequent and characteristic manifestation of scleroderma and sclerodermoid disorders, dermatologists are often the first-line doctors who must be able to promptly recognize skin symptoms to provide the affected patient a correct diagnosis and appropriate management.
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Em] Entry month:1707
[Cu] Class update date: 171124
[Lr] Last revision date:171124
[St] Status:In-Process
[do] DOI:10.1007/s12016-017-8625-4

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[PMID]: 28673091
[Au] Autor:Wong RX; Chia JC; Haber RM
[Ad] Address:1 Division of Dermatology, Cumming School of Medicine, Calgary, AB, Canada.
[Ti] Title:Review of Primary Cutaneous Mucinoses in Nonlupus Connective Tissue Diseases.
[So] Source:J Cutan Med Surg;:1203475417719053, 2017 Jul 01.
[Is] ISSN:1615-7109
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Lichen myxedematosus is an idiopathic, cutaneous mucinosis with 2 clinicopathologic subsets. There is the generalised papular and sclerodermoid form, more properly termed scleromyxedema, and the localised papular form. We report the first case, to our knowledge, of lichen myxedematosus in association with rheumatoid arthritis as well as a case in association with dermatomyositis. An up-to-date literature review on cutaneous mucinoses and connective tissue diseases, excluding the common association of primary and secondary mucinoses with systemic lupus erythematosus, was also performed.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1707
[Cu] Class update date: 170704
[Lr] Last revision date:170704
[St] Status:Publisher
[do] DOI:10.1177/1203475417719053

  5 / 593 MEDLINE  
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[PMID]: 28009441
[Au] Autor:Dore E; Swick BL; Link BK; Ghahramani GK; Liu V
[Ad] Address:Department of Dermatology, University of Iowa, Iowa City, Iowa.
[Ti] Title:Follicular lymphomatoid papulosis with follicular mucinosis: a clinicopathologic study of 3 cases with literature review and conceptual reappraisal.
[So] Source:J Cutan Pathol;44(4):360-366, 2017 Apr.
[Is] ISSN:1600-0560
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Lymphomatoid papulosis (LyP), characterized by recurring, waxing and waning, cutaneous papulonodules, is increasingly recognized to represent a heterogeneous collection of pathologically dissimilar subtypes. Recently, a follicular LyP variant was proposed, featuring folliculotropism. Folliculotropism by atypical lymphocytes is conventionally associated with follicular mucinosis and mycosis fungoides (MF), and review of the literature suggests co-occurrence of folliculotropism and follicular mucinosis in LyP to be rare, with only 3 cases identified to date. Herein we describe 3 additional cases, each manifesting a typical LyP clinical picture, with the additional element of folliculotropism and follicular mucinosis on pathology. These cases suggest that LyP should be considered alongside MF in the differential diagnosis of follicular mucinosis with accompanying atypical lymphocytic infiltration. As LyP can occur with other lymphoproliferative disorders such as MF, the finding of follicular mucinosis in LyP may further represent a conceptual intersection between the 2 disease processes.
[Mh] MeSH terms primary: Lymphomatoid Papulosis
Mucinosis, Follicular
Skin Neoplasms
[Mh] MeSH terms secundary: Adult
Aged
Female
Humans
Lymphomatoid Papulosis/metabolism
Lymphomatoid Papulosis/pathology
Mucinosis, Follicular/metabolism
Mucinosis, Follicular/pathology
Skin Neoplasms/metabolism
Skin Neoplasms/pathology
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Entry month:1706
[Cu] Class update date: 171121
[Lr] Last revision date:171121
[Js] Journal subset:IM
[Da] Date of entry for processing:161224
[St] Status:MEDLINE
[do] DOI:10.1111/cup.12871

  6 / 593 MEDLINE  
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[PMID]: 27450934
[Au] Autor:Kuo KL; Lee LY; Kuo TT
[Ad] Address:Department of Dermatology, Chang Gung Memorial Hospital, Keelung Branch, Keelung, Taiwan.
[Ti] Title:Solitary cutaneous focal mucinosis: A clinicopathological study of 11 cases of soft fibroma-like cutaneous mucinous lesions.
[So] Source:J Dermatol;44(3):335-338, 2017 Mar.
[Is] ISSN:1346-8138
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Cutaneous mucinoses encompass a variety of cutaneous disorders. Cutaneous focal mucinosis (CFM) was originally described as an asymptomatic solitary lesion characterized by abundant focal cutaneous mucin deposits. However, multiple focal mucinous lesions associated with systemic diseases have also been designated as CFM. Our clinicopathological study of 11 cases of solitary lesions confirmed that CFM is a unique primary cutaneous mucinosis unrelated to mucinosis-associated systemic diseases. We suggest calling this group of CFM lesions "solitary CFM" to distinguish them from multiple CFM associated with mucinosis associated systemic diseases. Our cases showed slight male predominance with a median age of 50 years. They occurred most often on the extremities (45%), presented as asymptomatic solitary, white to erythematous, small, soft, fibroma-like lesions. None of the clinical impressions were of CFM. We call attention to include solitary CFM in clinical differential diagnosis of polypoid skin lesions.
[Mh] MeSH terms primary: Mucinoses/pathology
Skin Diseases/pathology
[Mh] MeSH terms secundary: Adult
Aged
Diagnosis, Differential
Female
Fibroma/pathology
Humans
Male
Middle Aged
Mucinoses/diagnosis
Skin Diseases/diagnosis
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1703
[Cu] Class update date: 170306
[Lr] Last revision date:170306
[Js] Journal subset:IM
[Da] Date of entry for processing:160725
[St] Status:MEDLINE
[do] DOI:10.1111/1346-8138.13523

  7 / 593 MEDLINE  
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[PMID]: 27358105
[Au] Autor:Mitteldorf C; Rongioletti F; Kempf W; Tronnier M
[Ad] Address:Department of Dermatology, Venereology and Allergology, HELIOS-Klinikum Hildesheim, Hildesheim, Germany.
[Ti] Title:Papular mucinosis with monotypic plasma cells in a child.
[So] Source:J Eur Acad Dermatol Venereol;31(2):e89-e90, 2017 Feb.
[Is] ISSN:1468-3083
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Mucinoses/diagnosis
Plasma Cells/pathology
[Mh] MeSH terms secundary: Child
Female
Humans
Mucinoses/pathology
[Pt] Publication type:CASE REPORTS; LETTER
[Em] Entry month:1705
[Cu] Class update date: 170515
[Lr] Last revision date:170515
[Js] Journal subset:IM
[Da] Date of entry for processing:160701
[St] Status:MEDLINE
[do] DOI:10.1111/jdv.13784

  8 / 593 MEDLINE  
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[PMID]: 27336710
[Au] Autor:Williams RF; Hoang MP; Kroshinsky D; Smith GP
[Ad] Address:Mount Auburn Hospital, Boston, MA, USA.
[Ti] Title:Infliximab-induced follicular mucinosis of the face.
[So] Source:Int J Dermatol;56(2):215-217, 2017 Feb.
[Is] ISSN:1365-4632
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Drug Eruptions/etiology
Facial Dermatoses/chemically induced
Gastrointestinal Agents/adverse effects
Infliximab/adverse effects
Mucinosis, Follicular/chemically induced
[Mh] MeSH terms secundary: Adolescent
Crohn Disease/drug therapy
Female
Humans
Young Adult
[Pt] Publication type:CASE REPORTS
[Nm] Name of substance:0 (Gastrointestinal Agents); B72HH48FLU (Infliximab)
[Em] Entry month:1708
[Cu] Class update date: 170804
[Lr] Last revision date:170804
[Js] Journal subset:IM
[Da] Date of entry for processing:160624
[St] Status:MEDLINE
[do] DOI:10.1111/ijd.13335

  9 / 593 MEDLINE  
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[PMID]: 26805721
[Au] Autor:Atci T; Ekinci AP; Buyukbabani N; Baykal C
[Ad] Address:Departments of Dermatology & Venereology, Istanbul University Istanbul Medical Faculty, Istanbul, Turkey.
[Ti] Title:Reticular erythematous mucinosis on a mastectomy scar and relapse after mammary reconstruction.
[So] Source:J Eur Acad Dermatol Venereol;31(1):e13-e15, 2017 Jan.
[Is] ISSN:1468-3083
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Cicatrix/complications
Mastectomy/adverse effects
Mucinoses/etiology
Skin Diseases/etiology
[Mh] MeSH terms secundary: Female
Humans
Middle Aged
Recurrence
[Pt] Publication type:CASE REPORTS; LETTER
[Em] Entry month:1705
[Cu] Class update date: 170501
[Lr] Last revision date:170501
[Js] Journal subset:IM
[Da] Date of entry for processing:160126
[St] Status:MEDLINE
[do] DOI:10.1111/jdv.13585

  10 / 593 MEDLINE  
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ANBINDER, Ana Lia

[PMID]: 28329618
[Au] Autor:Narana Ribeiro El Achkar V; Posch Machado AC; Dias de Almeida J; Rodarte Carvalho Y; Anbinder AL
[Ad] Address:Department of Bioscience and Oral Diagnosis, Institute of Science and Technology, Univ. Estadual Paulista-UNESP, São José dos Campos, São Paulo. vivian.narana@gmail.com.
[Ti] Title:Oral focal mucinosis: review of the literature and two case reports.
[So] Source:Dermatol Online J;22(9), 2016 Sep 15.
[Is] ISSN:1087-2108
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Oral focal mucinosis is a rare condition, clinically characterized by an asymptomatic swelling, without distinct, specific features, which occurs predominantly in adults of the female gender. Its clinical aspect leads to various differential diagnoses, and final diagnosis is only possible by means of histopathological exam, in which a well-delimited myxomatous area containing mucinous material is observed. In the present study, a review of the English-language literature about the lesion, was conducted, covering the period from 1974 to March 2015. We report two new cases, thereby contributing to the knowledge and differential diagnosis of this entity.
[Mh] MeSH terms primary: Gingival Diseases/diagnosis
Mucinoses/diagnosis
[Mh] MeSH terms secundary: Adult
Female
Gingival Diseases/pathology
Humans
Male
Mouth Diseases/diagnosis
Mouth Diseases/pathology
Mucinoses/pathology
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Entry month:1710
[Cu] Class update date: 171011
[Lr] Last revision date:171011
[Js] Journal subset:IM
[Da] Date of entry for processing:170323
[St] Status:MEDLINE


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