Facial disfigurement due to osteitis fibrosa cystica or brown tumor from secondary hyperparathyroidism in patients on dialysis: A systematic review and an illustrative case report

被引:17
作者
Baracaldo, Rafael M. [1 ]
Bao, Dashi [1 ]
Iampornpipopchai, Pichet [1 ]
Fogel, Joshua [2 ]
Rubinstein, Sofia [1 ]
机构
[1] Nassau Univ Med Ctr, Div Nephrol & Hypertens, E Meadow, NY 11554 USA
[2] CUNY Brooklyn Coll, Dept Finance & Business Management, Brooklyn, NY 11210 USA
关键词
Brown tumors; craniofacial skeleton; dialysis; facial disfigurement; osteitis fibrosa cystica; secondary hyperparathyroidism; RENAL OSTEODYSTROPHY; LEONTIASIS-OSSEA; ALKALINE-PHOSPHATASE; TRANSPLANTATION; SPECTRUM; FAILURE; WOMEN; SEX;
D O I
10.1111/hdi.12298
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Osteitis fibrosa cystica (OFC) is the most frequent type of osseous change in renal osteodystrophy affecting the majority of dialysis patients. Brown tumors are a severe form of OFC. The involvement of the craniofacial skeleton causing facial disfigurement in patients on dialysis appears to be limited to case reports. After searching PubMed, we performed a systematic review of 127 cases with a severe form of OFC resulting in a facial disfigurement to understand possible determinants for this condition. We found that since the first published case in 1974, and after a peak in 1996, there appears to be an increase in published reported cases. Only 27.6% of these cases were published in nephrology journals. The most common region for reported cases was North America. Mean age of these patients was 31.2 years with a mean dialysis duration of 7 years. Almost 67% were women, and almost all were on hemodialysis. The disease tended to most commonly localize to the maxilla (73.2%) and mandible (57.5%). As part of the treatment, 59% of patients had a parathyroidectomy. More than one-third (35.4%) had symptomatic improvement at follow-up. Mean follow-up was 1.6 years. Clinicians should be aware of this clinical presentation of a severe form of OFC and/or brown tumors. Timely diagnosis and intervention may help to prevent or decrease destructive bone changes and reduce negative psychological consequences of facial disfigurement.
引用
收藏
页码:583 / 592
页数:10
相关论文
共 6 条
  • [1] Osteitis Fibrosa Cystica; A Forgotten Manifestation of Secondary Hyperparathyroidism Due to End-Stage Renal Disease: A Case Report
    Usmael, Semir Abdi
    Ansa, Sisay Molla
    Tufa, Derejie Woldesilasie
    INTERNATIONAL MEDICAL CASE REPORTS JOURNAL, 2022, 15 : 529 - 535
  • [2] Fine needle aspiration diagnosis of osteitis fibrosa cystica (brown tumor of bone): A case report
    Kemp, Anna M. Collins
    Bukvic, Mehila
    Sturgis, Charles D.
    ACTA CYTOLOGICA, 2008, 52 (04) : 471 - 474
  • [3] Secondary Hyperparathyroidism Presenting as a Brown Tumor: A Case Report and Review of the Literature
    Flores, Rui
    Lopes, Joana
    Caridade, Sofia
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (01)
  • [4] OSTEITIS-FIBROSA-CYSTICA (BROWN TUMOR) OF THE SPINE WITH CORD COMPRESSION - REPORT OF A CASE WITH NEEDLE ASPIRATION BIOPSY FINDINGS
    KASHKARI, S
    KELLY, TR
    BETHEM, D
    PEPE, RG
    DIAGNOSTIC CYTOPATHOLOGY, 1990, 6 (05) : 349 - 353
  • [5] Brown tumor in association with secondary hyperparathyroidism - A case report and review of the literature
    Pecovnik Balon, B
    Kavalar, R
    AMERICAN JOURNAL OF NEPHROLOGY, 1998, 18 (05) : 460 - 463
  • [6] Mandibular Brown Tumor as a Result of Secondary Hyperparathyroidism: A Case Report with 5 Years Follow-Up and Review of the Literature
    Shavlokhova, Veronika
    Goeppert, Benjamin
    Gaida, Matthias M.
    Saravi, Babak
    Weichel, Frederic
    Vollmer, Andreas
    Vollmer, Michael
    Freudlsperger, Christian
    Mertens, Christian
    Hoffmann, Juergen
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2021, 18 (14)