- Gastric Xanthoma in the Pediatric Population: A Possible Herald for Malignancy?
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Russell JD, Peck J, Phen C, Linehan JL, Karjoo S, Nguyen J, Wilsey MJ
- KMID: 2467900
- Pediatr Gastroenterol Hepatol Nutr.
- 2020 Jan;23(1):110-114.
- doi: 10.5223/pghn.2020.23.1.110
Gastric xanthoma is frequently an incidental finding on upper endoscopy in adults. Gastric xanthomas (GX) can be mistaken for malignancies and warrant prompt histologic diagnosis. The underlying etiology is not... -
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- Primary Histiocytic Sarcoma Presenting as a Breast Mass: A Case Report
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Bang S, Kim Y, Chung MS, Park JS, Choi YY, Shin SJ
- KMID: 2458869
- J Breast Cancer.
- 2019 Sep;22(3):491-496.
- doi: 10.4048/jbc.2019.22.e32
Histiocytic sarcoma is a rare hematologic malignancy, with very few cases of primary histiocytic sarcoma of the breast described in English scientific literature. Herein, we describe a case of primary... -
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- A Case of Rosai-Dorfman Disease Presented with Neck Mass
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Yoon HS, Kim DH, Kim MS, Ji YB
- KMID: 2451617
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2019 Jun;62(6):351-354.
- doi: 10.3342/kjorl-hns.2018.00339
Rosai-Dorfman disease, also known as the sinus histiocytosis with massive lymphadenopathy, is a rare and benign histioproliferative disease in which lymphadenopathy results from infiltration and dilatation of lymph node sinuses... -
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- Adult Xanthogranuloma: A Clinical, Histopathological, and Immunohistochemical Study of 19 Korean Cases
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Kwak HB, Jung ES, Park SW, Yun SK
- KMID: 2451585
- Korean J Dermatol.
- 2019 Jun;57(5):243-250.
BACKGROUND: Juvenile xanthogranuloma is a benign, self-limited disorder that usually occurs in infants and young children. Xanthogranuloma is rare in adults, and therefore studies reporting adult xanthogranuloma are limited. OBJECTIVE: We... -
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- Pigmented Villonodular Synovitis Developing in the Knee of a Rheumatoid Arthritis Patient Mistaken as a Rheumatoid Arthritis Flare-Up
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Lee SY, Lee SW, Chung WT
- KMID: 2438037
- Korean J Med.
- 2019 Feb;94(1):133-136.
- doi: 10.3904/kjm.2019.94.1.133
Pigmented villonodular synovitis is a benign tumor arising from synovial fibroblasts or histiocytes. There are diffuse and localized forms: the former involves the entire synovium and the latter consists of... -
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- IgG4-related Ophthalmic Disease Associated with Adult Xanthogranulomatous Disease
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Lee S, Chung S, Heo J, Lew H
- KMID: 2426369
- J Korean Ophthalmol Soc.
- 2018 Nov;59(11):1071-1076.
- doi: 10.3341/jkos.2018.59.11.1071
PURPOSE: To report a case of immunoglobulin G4 (IgG4)-related ophthalmic disease associated with adult xanthogranulomatous disease. CASE SUMMARY: A 38-year-old male with a history of cholecystectomy visited our clinic for bilateral... -
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- Bilateral Frosted Branch Angiitis in Kikuchi-Fujimoto Disease
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Kim HM, Choi YJ, Kim ST
- KMID: 2420338
- J Korean Ophthalmol Soc.
- 2018 Sep;59(9):876-880.
- doi: 10.3341/jkos.2018.59.9.876
PURPOSE: A case of frosted branch angiitis in Kikuchi-Fujimoto disease is reported. CASE SUMMARY: A 33-year-old male complained of a sudden decrease in visual acuity that developed in both eyes 5... -
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- Erdheim-Chester Disease Presenting as an Anterior Mediastinal Tumor without Skeletal Involvement
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Lee K, Kim HR, Roh J, Ok YJ, Jeon BB, Kim YW
- KMID: 2413067
- Korean J Thorac Cardiovasc Surg.
- 2018 Jun;51(3):223-226.
- doi: 10.5090/kjtcs.2018.51.3.223
Erdheim-Chester disease (ECD) is a form of non–Langerhans cell histiocytosis that most commonly involves the skeletal system. We report an unusual case of ECD presenting as an anterior mediastinal tumor... -
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- A Case of Erdheim-Chester Disease Developed during Treatment of Leukemia in a Child
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Hong JP, Ahn WK, Lim JY, Jung JE, Hahn SM, Han JW, Lyu CJ
- KMID: 2435427
- Clin Pediatr Hematol Oncol.
- 2018 Apr;25(1):66-70.
- doi: 10.15264/cpho.2018.25.1.66
Erdheim-Chester disease (ECD) is a rare non-Langerhan's cell histiocytosis disorder characterized by replacement of normal tissue by lipid-laden histiocytes affecting various organs. A few pediatric cases have been reported worldwide.... -
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- The Relation between Tympanostomy Tube Otorrhea and Types of Immune Cells in Middle Ear Effusion in Children with Otitis Media with Effusion
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Lim GC, Hyun CL, Kim DY, Choi SH, Song CI
- KMID: 2436438
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2018 Mar;61(3):133-138.
- doi: 10.3342/kjorl-hns.2017.00360
BACKGROUND AND OBJECTIVES: Tympanostomy tube insertion is one of the most common surgical procedures in children. Despite aseptic procedures with prophylactic antibiotic treatment, postoperative otorrhea may be encountered in some... -
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- Preoperative Cytologic Diagnosis of Warthin-like Variant of Papillary Thyroid Carcinoma
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Kim J, Lim BJ, Hong SW, Pyo JY
- KMID: 2408511
- J Pathol Transl Med.
- 2018 Mar;52(2):105-109.
- doi: 10.4132/jptm.2017.12.26
BACKGROUND: Warthin-like variant of papillary thyroid carcinoma (WLV-PTC) is a relatively rare variant of papillary thyroid carcinoma with favorable prognosis. However, preoperative diagnosis using fine-needle aspiration (FNA) specimens is challenging... -
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- Palisaded Neutrophilic and Granulomatous Dermatitis Manifested as a LE-nonspecific Skin Lesion
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Kim TH, Seo JW, Choi SH, Song KH, Kim KH
- KMID: 2401256
- Korean J Dermatol.
- 2017 Dec;55(10):684-688.
Palisaded neutrophilic and granulomatous dermatitis (PNGD) is a newly defined entity that includes various clinical entities. Histopathologically, this disease is characterized by a granulomatous inflammation with or without leukocytoclastic vasculitis.... -
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- Sclerema Neonatorum in a Full-Term Infant Showing Favorable Prognosis
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Park SH, Kim SC
- KMID: 2395191
- Ann Dermatol.
- 2017 Dec;29(6):790-793.
- doi: 10.5021/ad.2017.29.6.790
Sclerema neonatorum (SN) is a rare disease characterized by firm, indurated, waxy skin lesions extending throughout the body, sparing the fat-free soles, palms, and genitalia. The prognosis of SN is... -
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- Xanthogranulomatous pancreatitis mimicking potentially malignant pancreatic neoplasm: report of a case
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Kwon HJ
- KMID: 2397807
- Ann Hepatobiliary Pancreat Surg.
- 2017 Nov;21(4):243-246.
- doi: 10.14701/ahbps.2017.21.4.243
Xanthogranulomatous pancreatitis (XGP) is a rare benign disease that may mimic or accompany other pancreatic diseases. Here we report a case of XGP initially suspected as malignant cystic neoplasm of... -
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- Aggressive Indeterminate Dendritic Cell Tumor Mimicking Scalp Angiosarcoma
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Li Y, Wang TT, Zhang ZH, Wang L
- KMID: 2388914
- Ann Dermatol.
- 2017 Oct;29(5):614-617.
- doi: 10.5021/ad.2017.29.5.614
Indeterminate dendritic cell tumor (IDCT) is a proliferation of CD1a+, S100+ and langerin- histiocytes with a generally benign course. Here, we describe a case of a 90-year-old male who developed... -
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- A Case of Intralymphatic Histiocytosis Associated with Breast Cancer
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Kim JK, Kim MS, Na CH, Lee YS, Shin BS
- KMID: 2396217
- Korean J Dermatol.
- 2017 Sep;55(8):522-525.
Intralymphatic histiocytosis (IH) is a rare disease with variable and nonspecific clinical features, but with characteristic histopathological findings. Histopathologically, dilated lymphatic vessels containing aggregates of mononuclear cells are observed near... -
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- Severe Scrub Typhus with Hemophagocytic Lymphohistiocytosis Occurring in Summer
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Ahn JS, Noh JH, Kim HR, Jung J, Jo JC, Lim JH, Jun JB
- KMID: 2410197
- Korean J Med.
- 2017 Jun;92(3):321-325.
- doi: 10.3904/kjm.2017.92.3.321
In Korea, scrub typhus usually occurs in October and November. Hemophagocytic lymphohistiocytosis (HLH) is a distinct clinical entity characterized by a high fever, pancytopenia, hepatosplenomegaly, histiocyte proliferation, and hemophagocytosis. We... -
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- Rosai-Dorfman Disease of 4-Year-Old Girl
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Gang JS, Kim YC, Lee YM, Cho J, Suh WS, Park KB
- KMID: 2404887
- Soonchunhyang Med Sci.
- 2017 Jun;23(1):81-84.
- doi: 10.0000/sms.2017.23.1.81
Rosai-Dorfman disease also known as sinus histiocytosis with massive lymphadenopathy is a benign, rare systemic disease characterized by a histiocyte proliferation which presents with lymphadenopathy. We report a case of... -
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- Erdheim-Chester Disease with Emperipolesis: A Unique Case Involving the Heart
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Zhu P, Li N, Yu L, Miranda MN, Wang G, Duan Y
- KMID: 2378129
- Cancer Res Treat.
- 2017 Apr;49(2):553-558.
- doi: 10.4143/crt.2016.078
Histiocytosis is an uncommon disease characterized by excessive accumulation of histiocytes. Here, we report a rare case of non-Langerhans-cell histiocytosis in a 51-year-old woman who presented with severe symptoms of... -
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- A Case of Malignancy-associated Histiocytoid Sweet Syndrome in a Patient with AML
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Seo JW, Kim TH, Choi SH, Ha SM, Song KH, Kim KH
- KMID: 2371085
- Korean J Dermatol.
- 2017 Feb;55(2):124-128.
Sweet syndrome is a disorder characterized by painful, erythematous, cutaneous plaques and nodules of rapid onset accompanied by fever, leukocytosis, and neutrophilia. We encountered a case of a recurrent histiocytoid... -
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