Case of cutaneous botryomycosis in an 8-year-old immunocompetent boy with a review of the published work

被引:5
|
作者
Shimagaki, Haruna [1 ]
Yuki, Akihiko [1 ]
Kimura, Kiyoto [1 ]
Yuki, Daisuke [1 ]
Fujikawa, Hiroki [1 ]
Shimizu, Naoya [2 ]
Abe, Riichiro [1 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Dermatol, Niigata, Japan
[2] Shindaiekimaehifuka, Div Dermatol, Niigata, Japan
来源
JOURNAL OF DERMATOLOGY | 2020年 / 47卷 / 05期
关键词
Bollinger granules; botryomycosis; cutaneous infection; immunocompetent child; Splendore-Hoeppli phenomenon;
D O I
10.1111/1346-8138.15308
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Botryomycosis is a rare chronic suppurative granulomatous infection caused by several genera of non-filamentous bacteria. The clinical and histopathological findings are similar to those of mycetoma caused by true fungi or aerobic actinomycetes. Botryomycosis is divided into cutaneous and visceral disease, with the cutaneous form being more common. Histopathology shows granules of etiologic bacteria called "sulfur granules". Botryomycosis occurs more commonly among immunocompromised patients, although some cases have also been reported in immunocompetent patients. We report the case of an 8-year-old immunocompetent boy who visited our hospital with a 4-mm diameter subcutaneous tumor with mild tenderness on his right heel for several months. We surgically removed the tumor with an initial diagnosis of epidermal cyst. Histopathology showed sulfur granules surrounded by an eosinophilic matrix, indicating the Splendore-Hoeppli phenomenon. The granules consisted of Gram-positive cocci, leading to a diagnosis of botryomycosis. The patient was successfully treated by excision and oral trimethoprim/sulfamethoxazole (240 mg b.i.d.) for 2 weeks as adjuvant therapy. No recurrence was noted following treatment. The subcutaneous tumor in this case was smaller than the typical in botryomycosis infections. We reviewed the infection duration and tumor size in reported cases of botryomycosis in immunocompetent patients. Small tumor size may suggest that the case is in an early stage; therefore, it is important to remove and investigate these lesions proactively.
引用
收藏
页码:542 / 545
页数:4
相关论文
共 50 条
  • [31] 8-YEAR-OLD BOY WITH PROGRESSIVE HEADACHE
    Hervey-Jumper, Shawn L.
    Wang, Anthony C.
    Yates, Andrea N.
    Robertson, Patricia L.
    Muraszko, Karin M.
    Garton, Hugh J. L.
    Blaivas, Mila
    BRAIN PATHOLOGY, 2013, 23 (05) : 601 - 602
  • [32] Case 3: Fever and Back Pain in an 8-year-old Boy
    Elder, Theresa A.
    Talati, Sanjay J.
    Moore, Mary D.
    PEDIATRICS IN REVIEW, 2020, 41 (04) : 203 - +
  • [33] Gastroesophageal reflux disease in an 8-year-old boy: A case study
    Jonasson, AK
    Knaap, SFC
    JOURNAL OF MANIPULATIVE AND PHYSIOLOGICAL THERAPEUTICS, 2006, 29 (03) : 245 - 247
  • [34] Case report: an 8-year-old boy with unusual retinal hyperpigmentation
    Syed, R. N.
    Ghosh, Y.
    Berry-Brincat, A.
    Gregory, M. E.
    Brown, R.
    EYE, 2006, 20 (09) : 1076 - 1078
  • [35] Cementoblastoma Arising in the Maxilla of an 8-Year-Old Boy: A Case Report
    Harada, Hiroyuki
    Omura, Ken
    Mogi, Seiki
    Okada, Norihiko
    INTERNATIONAL JOURNAL OF DENTISTRY, 2011, 2011
  • [36] Case report: An 8-year-old boy with unusual retinal hyperpigmentation
    R N Syed
    Y Ghosh
    A Berry-Brincat
    M E Gregory
    R Brown
    Eye, 2006, 20 : 1076 - 1078
  • [37] Necrotic acalculous cholecystitis in an 8-year-old boy: a case report
    Mueller, Fanny
    Mcdonald, Amy
    Schellerer, Vera S.
    JOURNAL OF MEDICAL CASE REPORTS, 2025, 19 (01)
  • [38] Cat scratch disease in a 8-year-old boy - a case report
    Pawlowska-Iwanicka, Kamila
    Podsiadlowicz-Borzecka, Malgorzata
    Stelmach, Iwona
    PEDIATRIA I MEDYCYNA RODZINNA-PAEDIATRICS AND FAMILY MEDICINE, 2016, 12 (04): : 451 - 454
  • [39] A Case Report of ROHHAD Syndrome in an 8-year-old Iranian Boy
    Amjadipour, Abolfazl
    Shahkar, Lobat
    Hanafi, Faridreza
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2021, 19 (03)
  • [40] ACHALASIA IN AN 8-YEAR-OLD BOY WITH ASTHMA SYMPTOMS: A CASE REPORT
    Khue, B. D.
    Thuan, L. T.
    Lan, L. T. Tuyet
    RESPIROLOGY, 2011, 16 : 224 - 225