Database : MEDLINE
Search on : Angiolymphoid and Hyperplasia and with and Eosinophilia [Words]
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[PMID]: 29182841
[Au] Autor:Inanaga R; Shimizu H; Uchida H; Kataoka I; Kobayashi M; Fukuoka K; Karube M; Komagata Y; Kaname S; Arimura Y
[Ti] Title:[A case report of a nephrotic syndrome on IgA nephropathy complicated by Kimura's disease.]
[So] Source:Nihon Naika Gakkai Zasshi;105(5):881-885, 2016 May.
[Is] ISSN:0021-5384
[Cp] Country of publication:Japan
[La] Language:jpn
[Mh] MeSH terms primary: Angiolymphoid Hyperplasia with Eosinophilia/complications
Glomerulonephritis, IGA/complications
Nephrotic Syndrome/etiology
[Mh] MeSH terms secundary: Humans
Male
Middle Aged
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180214
[Lr] Last revision date:180214
[Js] Journal subset:IM
[Da] Date of entry for processing:171129
[St] Status:MEDLINE

  2 / 946 MEDLINE  
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[PMID]: 29402550
[Au] Autor:Ribeiro L; Souto M; Loureiro A
[Ad] Address:Department of Pulmonology, Centro Hospitalar de Trás-os-Montes e Alto Douro, Vila Real, Portugal. Electronic address: liliana.sc.ribeiro@hotmail.com.
[Ti] Title:Angiolymphoid Hyperplasia With Eosinophilia of the Lung.
[So] Source:Arch Bronconeumol;, 2018 Feb 02.
[Is] ISSN:1579-2129
[Cp] Country of publication:Spain
[La] Language:eng; spa
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180206
[Lr] Last revision date:180206
[St] Status:Publisher

  3 / 946 MEDLINE  
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SciELO Brazil full text

[PMID]: 29186256
[Au] Autor:Bastos JT; Rocha CRMD; Silva PMCE; Freitas BMP; Cassia FF; Avelleira JCR
[Ad] Address:Department of Dermatology at Hospital Federal da Lagoa - Rio de Janeiro (RJ), Brazil.
[Ti] Title:Angiolymphoid hyperplasia with eosinophilia versus Kimura's disease: a case report and a clinical and histopathological comparison.
[So] Source:An Bras Dermatol;92(3):392-394, 2017 May-Jun.
[Is] ISSN:1806-4841
[Cp] Country of publication:Brazil
[La] Language:eng
[Ab] Abstract:Angiolymphoid hyperplasia with eosinophilia is a rare and benign vascular tumor whose etiology remains uncertain. It clinically presents itself by angiomatous papules or nodules located on the head and neck. Many controversies in the literature are found in relation to angiolymphoid hyperplasia with eosinophilia and Kimura's disease - its main differential diagnosis - due to their clinical and histopathological similarities. However, currently, most studies agree that they are distinct diseases. The present case illustrates a characteristic description of angiolymphoid hyperplasia with eosinophilia and also highlights the main differences with Kimura's disease.
[Mh] MeSH terms primary: Angiolymphoid Hyperplasia with Eosinophilia/pathology
Scalp Dermatoses/pathology
[Mh] MeSH terms secundary: Aged
Angiolymphoid Hyperplasia with Eosinophilia/diagnosis
Diagnosis, Differential
Female
Humans
Scalp Dermatoses/diagnosis
[Pt] Publication type:CASE REPORTS
[Em] Entry month:1801
[Cu] Class update date: 180131
[Lr] Last revision date:180131
[Js] Journal subset:IM
[Da] Date of entry for processing:171130
[St] Status:MEDLINE

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[PMID]: 28468187
[Au] Autor:Sharma R
[Ad] Address:Oral and Maxillofacial Surgery, Armed Forces Medical College, Pune, India.
[Ti] Title:Superficial Parotidectomy Plane for Debulking Surgery in Kimura Disease.
[So] Source:J Craniofac Surg;28(3):e207-e208, 2017 May.
[Is] ISSN:1536-3732
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Kimura disease (KD) is a rare chronic inflammatory disorder of unknown etiology representing as solitary or multiple subcutaneous nodules predominantly in the head and neck region. Common sites of involvement are preauricular region, forehead and scalp. The soft tissue localization is often associated with regional lymphadenopathy and enlargement of the major salivary gland. The authors report a patient with KD involving the right parotid and left temporal region managed successfully at our center using a combination of debulking superficial parotidectomy and medicinal therapy. To the best of knowledge of the authors, this is the first completely esthetically treated patient with KD with no clinical evidence of residual disease.
[Mh] MeSH terms primary: Angiolymphoid Hyperplasia with Eosinophilia/surgery
Cytoreduction Surgical Procedures/methods
Parotid Gland/surgery
[Mh] MeSH terms secundary: Angiolymphoid Hyperplasia with Eosinophilia/diagnosis
Humans
Male
Parotid Neoplasms/surgery
Young Adult
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1801
[Cu] Class update date: 180126
[Lr] Last revision date:180126
[Js] Journal subset:D
[Da] Date of entry for processing:170505
[St] Status:MEDLINE
[do] DOI:10.1097/SCS.0000000000003387

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[PMID]: 29310412
[Au] Autor:Lee DH; Kim GE; Yang E; Yoon TM; Lee JK; Lim SC
[Ad] Address:Department of Otolaryngology-Head and Neck Surgery.
[Ti] Title:Kimura disease of buccal region in a pediatric patient with nephrotic syndrome: A case report.
[So] Source:Medicine (Baltimore);96(48):e8990, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:RATIONALE: Kimura disease is a rare benign, chronic inflammatory disorder that typically presents with slowly enlarging, nontender, subcutaneous swellings in the head and neck region. The occurrence of Kimura disease in the oral cavity is extremely rare. PATIENT CONCERNS: A 16-year-old boy presented with a complaint of a right painless buccal mass of 3 years' duration. DIAGNOSIS: The patient had been diagnosed with nephrotic syndrome and treated with corticosteroid at the age of 5 years. OUTCOMES: We report an extremely rare case of Kimura disease of the buccal region in a 16-year-old boy with nephrotic syndrome. LESSON: We controlled Kimura disease and nephrotic syndrome in this patient by using a combination of surgical resection of the buccal mass and systemic steroid therapy.
[Mh] MeSH terms primary: Angiolymphoid Hyperplasia with Eosinophilia/complications
Nephrotic Syndrome/complications
[Mh] MeSH terms secundary: Adolescent
Adrenal Cortex Hormones/therapeutic use
Angiolymphoid Hyperplasia with Eosinophilia/drug therapy
Angiolymphoid Hyperplasia with Eosinophilia/pathology
Angiolymphoid Hyperplasia with Eosinophilia/surgery
Cheek/diagnostic imaging
Cheek/pathology
Cheek/surgery
Humans
Male
Nephrotic Syndrome/diagnostic imaging
Nephrotic Syndrome/drug therapy
Nephrotic Syndrome/pathology
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Nm] Name of substance:0 (Adrenal Cortex Hormones)
[Em] Entry month:1801
[Cu] Class update date: 180116
[Lr] Last revision date:180116
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:180110
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008990

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[PMID]: 29266025
[Au] Autor:Llamas-Velasco M; Kempf W; Cota C; Fernández-Figueras MT; Lee J; Ferrara G; Sander C; Shapiro PE; Requena L; Kutzner H
[Ad] Address:Dermatology Department, Hospital Universitario de la Princesa.
[Ti] Title:Multiple Eruptive Epithelioid Hemangiomas: A Subset of Cutaneous Cellular Epithelioid Hemangioma With Expression of FOS-B.
[So] Source:Am J Surg Pathol;, 2017 Dec 20.
[Is] ISSN:1532-0979
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:There is a wide clinicopathologic spectrum of vascular proliferations characterized by the presence of epithelioid endothelial cells, comprising epithelioid hemangioma (EH)-pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma (PM-HAE), epithelioid hemangioendothelioma, and epithelioid angiosarcoma. Immunohistochemical FOS-B expression as well as FOS-B rearrangement (fluorescent in situ hybridization [FISH]) have recently been described as diagnostically relevant underpinnings of EH (restricted to osseous lesions) and PM-HAE. The aim of this study was to clinicopathologically characterize and to elucidate FOS-B expression in patients with eruptive lesions of the cellular variant of cutaneous EH. All cases of cutaneous cellular EH (n=16) showed strong diffuse immunohistochemical expression of FOS-B, in conjunction with positivity for ERG and nestin. Expression of MYC, CAMTA-1, AE1/3, and MNF116 was negative in all cases. FISH investigations did not show any sign of rearrangements for CAMTA-1 or MYC amplification. Negative-control cases included 15 lobular hemangiomas, 5 epithelioid angiosarcomas, and 5 nodular Kaposi sarcomas, all of which were negative for FOS-B. Positive-control cases included 15 angiolymphoid hyperplasia with eosinophilia cases, all of them being positive. In contrast with what has been published so far, cutaneous variants of cellular EH exhibit positive immunostaining for FOS-B. Remarkably, FOS-B expression is not restricted to the intraosseous subset of EH. For differential diagnosis of epithelioid vascular tumors, we therefore suggest a helpful panel of antibodies including CAMTA-1, TFE-3, FOS-B, and AE1/AE3. We point out the telltale immunophenotypes: angiolymphoid hyperplasia with eosinophilia and EH (FOS-B/others negative), PM-HAE (FOS-B/AE1/AE3/others negative), epithelioid hemangioendothelioma (CAMTA-1 or TFE-3/others negative). Remarkably, MYC is not expressed in these tumors, neither is there an MYC amplification by FISH. We suggest the term multiple eruptive EHs for this subset of cutaneous vascular tumors.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171221
[Lr] Last revision date:171221
[St] Status:Publisher
[do] DOI:10.1097/PAS.0000000000001003

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[PMID]: 29141835
[Au] Autor:Ito A; Sugita K; Tsutsumi R; Yamamoto O
[Ad] Address:Division of Dermatology, Department of Medicine of Sensory and Motor Organs, Tottori University Faculty of Medicine, Yonago, Japan.
[Ti] Title:Angiolymphoid hyperplasia with eosinophilia on the abdomen with dendritic cell infiltration.
[So] Source:Eur J Dermatol;, 2017 Nov 15.
[Is] ISSN:1952-4013
[Cp] Country of publication:France
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1711
[Cu] Class update date: 171116
[Lr] Last revision date:171116
[St] Status:Publisher
[do] DOI:10.1684/ejd.2017.3148

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[PMID]: 29057451
[Au] Autor:Bahloul E; Amouri M; Charfi S; Boudawara O; Mnif H; Boudawara T; Turki H
[Ad] Address:Department of Dermatology, Hedi Chaker Hospital, Sfax, Tunisia.
[Ti] Title:Angiolymphoid hyperplasia with eosinophilia: report of nine cases.
[So] Source:Int J Dermatol;56(12):1373-1378, 2017 Dec.
[Is] ISSN:1365-4632
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:BACKGROUND: Angiolymphoid hyperplasia with eosinophilia (ALHE) is a benign vascular proliferation characterized by dermal or subcutaneous red or brown papules or nodules, most commonly on the head and neck. OBJECTIVE: The aim of this study was to review the epidemiological and clinical characteristics of ALHE, focusing particularly on the histological and therapeutic features. METHODS: We performed a retrospective study of all cases of ALHE diagnosed in our dermatology and pathology departments between 2004 and 2015. RESULTS: Over 12 years, we collected nine cases of ALHE (0.75 case/year). There were four men and five women. The mean age was 43 years. Lesions presented as erythematous or violaceous papules or nodules in all cases, multiple in five cases, and localized on the head in eight cases or other sites in four cases. The diagnosis of ALHE was clinically suspected in only two cases. The histopathological findings showed an ill-circumscribed, intradermal slightly lobular proliferation of capillary-sized vessels around several central vessels. In all cases, the blood vessels were lined by large endothelial cells. An inflammatory infiltrate around the vessels was formed mainly of lymphocytes and eosinophils with isolated plasma cells and histiocytes. Surgery was the most common treatment in our series. Other local or general treatment has also been used with varying responses. CONCLUSION: Angiolymphoid hyperplasia with eosinophilia is a rare epithelioid vascular tumor with a challenging clinical and histological diagnosis. Despite its benign nature, ALHE causes a therapeutic dilemma.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1710
[Cu] Class update date: 171113
[Lr] Last revision date:171113
[St] Status:In-Process
[do] DOI:10.1111/ijd.13800

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[PMID]: 28946727
[Au] Autor:Woo SH; Kim HK; Kim WS; Bae TH; Kim MK
[Ad] Address:Department of Plastic and Reconstructive Surgery, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea.
[Ti] Title:A Rare Case of Kimura Disease with Bilateral Parotid Involvement.
[So] Source:Arch Plast Surg;44(5):439-443, 2017 Sep.
[Is] ISSN:2234-6163
[Cp] Country of publication:Korea (South)
[La] Language:eng
[Ab] Abstract:Kimura disease is a rare idiopathic chronic inflammatory disorder. It typically presents in the head and neck area, whereas bilateral involvement is unusual. Its diagnosis requires it to be differentiated from other inflammatory diseases and from head and neck tumors. Treatment methods include conservative management, steroid administration, radiotherapy, and surgery; however, no single treatment of choice has been established. Herein, we report an unusual presentation of Kimura disease with bilateral parotid involvement. This case was treated by surgical excision.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1709
[Cu] Class update date: 171008
[Lr] Last revision date:171008
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.5999/aps.2017.44.5.439

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[PMID]: 28932783
[Au] Autor:Shah K; Tran AN; Magro CM; Zang JB
[Ad] Address:Department of Dermatology, Weill Cornell Medicine, New York, New York.
[Ti] Title:Treatment of Kimura disease with mycophenolate mofetil monotherapy.
[So] Source:JAAD Case Rep;3(5):416-419, 2017 Sep.
[Is] ISSN:2352-5126
[Cp] Country of publication:United States
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1709
[Cu] Class update date: 170924
[Lr] Last revision date:170924
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.1016/j.jdcr.2017.04.010


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