• Title/Summary/Keyword: Angiolymphoid hyperplasia with eosinophilia

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Angiolymphoid Hyperplasia with Eosinophilia (ALHE) of the Oral Cavity: a Case Report (구강내에 발생한 혈관림프증식증: 증례보고)

  • Cho, Dong-Baek;Park, Ji-Un;Baek, Ji-Young;Choi, Won-Sik
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.32 no.6
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    • pp.573-576
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    • 2010
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign vascular lesion that is characterized by proliferation of small to medium-sized vascular structures lined by histiocytoid or epithelioid endothelial cells and often accompanied by an inflammatory infiltrate comprising lymphocytes, plasma cells and eosinophils. A 34-year-old man without any generalized systemic conditions presented with a slowly enlarging painless swelling in the buccal area. An excisional biopsy was conducted and the diagnosis of Angiolymphoid hyperplasia with eosinophilia was confirmed. We report a case of angiolymphoid hyperplasia with eosinophilia of the buccal area in oral cavity and review the previously reported cases and literatures of angiolymphoid hyperplasia with eosinophilia.

Angiolymphoid Hyperplasia with Eosinophilia mimicking Parotid Tumor (이하선 부위에 발생한 Angiolymphoid Hyperplasia with Eosinophilia)

  • Kim, Que-Chic;Noh, He-Il;Auo, Hyeon-Jin;Chun, Byung-Joon;Cho, Jung-Hae;Kang, Seok-Jin
    • Korean Journal of Bronchoesophagology
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    • v.8 no.2
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    • pp.51-55
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    • 2002
  • Angiolymphoid hyperplasia with eosinophilia(ALHE) is an uncommon idiopathic condition that presents with isolatedor grouped cutaneous plaques or nodules of the head and neck. Extracutaneous involvement is rare. ALHE is a distinct pathologic entity marked by a proliferation of blood vessels with distinctive large endothelial cells accompanied by a characteristic inflammatory infiltrate that includes eosinophils. The lesion is benign but may be persistent and difficult to eradicate. The authors have recently experiecned a case of angiolymphoid hyperplasia with eosinophilia in a 52-year-old male who had a painless enlarging mass in his right preauricular area and external ear canal for several years. We present this case with the review of literatures.

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ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA : A CASE REPORT (호산구 증가중을 동반한 ANGIOLYMPHOID HYPERPLASIA의 증례보고)

  • Kim, Young-Kyun;Yeo, Hwan-Ho;Lee, Cheol-Woo;Yang, In-Seok;Cho, Se-In;Cho, Jae-O
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.15 no.1
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    • pp.27-34
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    • 1993
  • Angiolymphoid hyperplasia with eosinophilia is an unusual and controversial lesion that occurs primarily in the head and neck area. This lesion was usually confused with Kimura's disease. We present the case of a 32-year-old woman with massive soft movable mass in left facial area which was diagnosed preoperatively as a fasciitis nodular. The final histologic diagnosis of the excised mass was angiolymphoid hyperplasia with eosinophilia(ALHE).

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THE CASE REPORT OF ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA ON CHIN (하악 이부에 생긴 Angiolymphoid hyperplasia with eosinophilia(Kimura's disease)의 치험례)

  • Yang, Yun-Seok;Cho, Yong-Seok
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.18 no.3
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    • pp.443-447
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    • 1996
  • Angiolymphoid hyperplasia with eosinophilia(ALHE) is an uncommon, benign vascular proliferation with the background of a stroma which is heavily infiltrated by lymphocytes and eosinophils and includes lymphatic follicles with prominent germinal centers. ALHE primarily involves the skin and subcutis in head and neck as various forms of nodules. There has been considerable controversy about the relationship between ALHE and Kimura's disease. Kimura's disease, originally reported by Kimura et el., is an unusual granulation with proliferation of lymphoid tissue. Wells and Whimster published the first report describing a condition that resembled Kimura's disease and designated it as ALHE. For a time being two lesions are thought to be same lesion, but recently they are considered as two different entities, histopathologically. The cause of this disease remains unknown, and physicians have used a variety of treatment modalities including cryosurgery, steriod therapy, electrodesiccation, curettage, radiotherapy, laser therapy and surgical excision. But any treatment modality leaves problem of recurrence because the lesion is not well encapsulated. Being poorly encapsulated, the lesion's remnants are apt to be left and this markes some problems : recurrence and possible adjacent organ injury. In this case we misdiagnosed the lesion as well encapsulated benign mass. We performed excisional biopsy and experienced prolonged operation time and unwanted mentalis muscle injury. We think that the importance of poor encapsulation of ALHE should be stressed. So we report our experience with literature review.

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Angiolymphoid hyperplasia with eosinophilia attached to the masseter muscle

  • Kwon, Hyo Jeong;Jung, Ee Room;Choi, Jong Yun;Seo, Bommie Florence;Kwon, Ho;Jung, Sung-No
    • Archives of Craniofacial Surgery
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    • v.21 no.5
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    • pp.319-322
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    • 2020
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign vascular tumor. The pathogenesis of ALHE is unknown; however, it may be linked to local trauma. ALHE predominantly occurs in areas of the preauricular region, forehead, and scalp; the masseter area is rarely involved. A 49-year-old man was referred for a mass in the right cheek region that was felt 2 months prior. Physical and imaging examination results suggested the presence of a benign tumor. Thus, surgical excision was performed. Pathologic findings confirmed an unexpected diagnosis of ALHE. This case was interesting, since the mass occurred at an unusual site with a misdiagnosis of an epidermal inclusion cyst.

Sequentially Developed Bilateral Postauricular Kimura's Disease (시차를 두고 양측 후이개에 발생한 기무라씨병 1예)

  • Lee, Yong Ju;Kim, Chang Yong;Nahm, Ji Hae;Park, Soon Hyung
    • Korean Journal of Head & Neck Oncology
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    • v.29 no.1
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    • pp.22-25
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    • 2013
  • Angiolymphoid hyperplasia with eosinophilia(Kimura's disease) is a relatively uncommon chronic benign disorder of unknown etiology, predominantly in the head and neck region and associated with lymphadenopathy or salivary gland enlargement. The treatment options are still controversial including medical therapy, surgery, and radiation. Kimura's disease of bilateral postauricular involvement has rarely been reported. We report a male patient with sequentially developed Kimura's disease involving the bilateral postauricular region and was treated by combined surgical excision and steroid therapy.

A Case of Kimura's disease (경부에 발생한 기무라씨병 1례)

  • 김춘일;김상후;정대건;박용수
    • Korean Journal of Bronchoesophagology
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    • v.3 no.2
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    • pp.323-326
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    • 1997
  • Kimura's disease is a chronic inflammatory disease which often presents as a tumor like swelling in the head and neck region. This lesion is benign but it may easily be mistaken for a malignant tumor. Kimura's disease has been confused with angiolymphoid hyperplasia with eosinophilia(ALHE). The cause is unknown, but theories include autoimmune, allergic, neoplastic, and infectious cause by insect bites and parasites. The treatment of choice is surgical removal. Recently we experienced a case of Kimura's disease occuring in the both side of posterior neck triangle area of a 37 year old male patient who was treated with surgical excision and systemic corticosteroid administration.

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RECURRED ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA (호산구증가증을 동반한 혈관임파양 증식증)

  • Byun, Young-Nam;Kim, Jong-Chul;Choung, Pill-Hoon;Yoon, Young-Ho
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.18 no.4
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    • pp.636-646
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    • 1996
  • Angiolymphoid hyperplasia with eosinophilia(ALHE) is a benign subcutaneous lesion that primarily affects head and neck region. It is characterized by single or multiple nodules in the subcutaneous tissue associated with eosinophilia in the peripheral blood. Kimura's disease, originally reported by Kimura et al., is similar lesion with ALHE in the clinical and histopathological aspects. There has been considerable controversy about the relation between Kimura's disease and ALHE. In Korea, 26 cases of Kimura's disease and ALHE have been reported since 1975. We present a case of recurred ALHE occurring on the left cheek in a 58-year-old woman. Including this case, we summarized all cases that were reported as Kimura's disease or ALHE in Korea through literature review. We also give an outline of clinical and histopathological characteristics of cases reported in Korea.

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A Case of Immunoglobulin A Nephropathy in a Patient with Kimura's Disease

  • Park, Hye Jung;Kim, Jae Kyung;Kim, Hyun Ju;Park, Kwan-Kyu;Bae, Yoon Sung;Lee, Yong Kyu;Kim, Beom Seok
    • Journal of Yeungnam Medical Science
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    • v.30 no.2
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    • pp.149-151
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    • 2013
  • Kimura's disease is an angiolymphoid-proliferative disorder that manifests with benign subcutaneous swelling predominantly in the head and the neck. Kidney involvement, including proteinuria, occurs in 12-16% of patients with the disease, and 60-78% of such cases is nephrotic syndrome. Reported etiologies of nephrotic syndrome in Kimura's disease include membranous glomerulonephritis, mesangial proliferative glomerulonephritis, minimal-change disease, focal segmental glomerulosclerosis, diffuse proliferative glomerulonephritis and immunoglobulin A (IgA) nephropathy. There have been only two case reports of IgA nephropathy in Kimura's disease, in 1998. In this report, we present a third case of IgA nephropathy associated with Kimura's disease.

A Rare Case of Kimura Disease with Bilateral Parotid Involvement

  • Woo, Soo Hyun;Kim, Han Koo;Kim, Woo Seob;Bae, Tae Hui;Kim, Mi Kyung
    • Archives of Plastic Surgery
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    • v.44 no.5
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    • pp.439-443
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    • 2017
  • 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.