Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

438 results
Display

Gastric Xanthoma in the Pediatric Population: A Possible Herald for Malignancy?

Russell JD, Peck J, Phen C, Linehan JL, Karjoo S, Nguyen J, Wilsey MJ

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Primary Histiocytic Sarcoma Presenting as a Breast Mass: A Case Report

Bang S, Kim Y, Chung MS, Park JS, Choi YY, Shin SJ

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Rosai-Dorfman Disease Presented with Neck Mass

Yoon HS, Kim DH, Kim MS, Ji YB

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Adult Xanthogranuloma: A Clinical, Histopathological, and Immunohistochemical Study of 19 Korean Cases

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pigmented Villonodular Synovitis Developing in the Knee of a Rheumatoid Arthritis Patient Mistaken as a Rheumatoid Arthritis Flare-Up

Lee SY, Lee SW, Chung WT

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
IgG4-related Ophthalmic Disease Associated with Adult Xanthogranulomatous Disease

Lee S, Chung S, Heo J, Lew H

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bilateral Frosted Branch Angiitis in Kikuchi-Fujimoto Disease

Kim HM, Choi YJ, Kim ST

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Erdheim-Chester Disease Presenting as an Anterior Mediastinal Tumor without Skeletal Involvement

Lee K, Kim HR, Roh J, Ok YJ, Jeon BB, Kim YW

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Erdheim-Chester Disease Developed during Treatment of Leukemia in a Child

Hong JP, Ahn WK, Lim JY, Jung JE, Hahn SM, Han JW, Lyu CJ

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....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Relation between Tympanostomy Tube Otorrhea and Types of Immune Cells in Middle Ear Effusion in Children with Otitis Media with Effusion

Lim GC, Hyun CL, Kim DY, Choi SH, Song CI

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Preoperative Cytologic Diagnosis of Warthin-like Variant of Papillary Thyroid Carcinoma

Kim J, Lim BJ, Hong SW, Pyo JY

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Palisaded Neutrophilic and Granulomatous Dermatitis Manifested as a LE-nonspecific Skin Lesion

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....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Sclerema Neonatorum in a Full-Term Infant Showing Favorable Prognosis

Park SH, Kim SC

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Xanthogranulomatous pancreatitis mimicking potentially malignant pancreatic neoplasm: report of a case

Kwon HJ

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Aggressive Indeterminate Dendritic Cell Tumor Mimicking Scalp Angiosarcoma

Li Y, Wang TT, Zhang ZH, Wang L

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Intralymphatic Histiocytosis Associated with Breast Cancer

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Severe Scrub Typhus with Hemophagocytic Lymphohistiocytosis Occurring in Summer

Ahn JS, Noh JH, Kim HR, Jung J, Jo JC, Lim JH, Jun JB

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Rosai-Dorfman Disease of 4-Year-Old Girl

Gang JS, Kim YC, Lee YM, Cho J, Suh WS, Park KB

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Erdheim-Chester Disease with Emperipolesis: A Unique Case Involving the Heart

Zhu P, Li N, Yu L, Miranda MN, Wang G, Duan Y

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Malignancy-associated Histiocytoid Sweet Syndrome in a Patient with AML

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2023 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr