Ophthalmic Rosai-Dorfman disease: a multi-centre comprehensive study

被引:9
作者
Alzahem, Tariq A. [1 ,2 ]
Cruz, Antonio Augusto [3 ]
Maktabi, Azza M. Y. [4 ]
Chahud, Fernando [5 ]
Alkatan, Hind [6 ,7 ]
机构
[1] King Khalid Eye Specialist Hosp, Vitreoretinal Div, Riyadh, Saudi Arabia
[2] King Saud Univ, King Saud Univ Med City, Coll Med, Ophthalmol Dept, Riyadh, Saudi Arabia
[3] Univ Sao Paulo, Sch Med Ribeirao Preto, Ophthalmol Dept, Sao Paulo, Brazil
[4] King Khalid Eye Specialist Hosp, Pathol & Lab Med Dept, Riyadh, Saudi Arabia
[5] Univ Sao Paulo, Sch Med Ribeirao Preto, Pathol Dept, Sao Paulo, Brazil
[6] King Saud Univ, Coll Med, Dept Ophthalmol, POB 266, Riyadh 11362, Saudi Arabia
[7] King Saud Univ, Coll Med, Pathol & Lab Med Dept, Riyadh, Saudi Arabia
关键词
Rosai-Dorfman disease; Orbit; Familial; Histopathology; Lymphadenopathy; SINUS HISTIOCYTOSIS; MASSIVE LYMPHADENOPATHY; MANIFESTATIONS; MIMICKING; SPECTRUM; LESIONS;
D O I
10.1186/s12886-021-02173-1
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background To provide basic demographic information and clinicopathologic features of ophthalmic Rosai-Dorfman disease (RDD) with a literature review. Methods A multi-centre retrospective case series reviewing all patients with histopathologically confirmed ophthalmic RDD at three tertiary eye care centres between January 1993 and December 2018. Results Eleven eyes of eight patients with histopathologically confirmed ophthalmic RDD were included, with equal numbers of males and females. The median age was 40.25 years (range: 26.6-72.4). Two patients had familial RDD. The orbit was the most commonly involved site (90.9% eyes). One patient (one eye) presented with a scleral nodule, anterior uveitis and cystoid macular oedema. Visual acuity ranged from 20/25 to light perception. Six patients had an extra-nodal ophthalmic disease, and the remaining two had an associated submandibular lymphadenopathy (nodal RDD). Conclusions Ophthalmic RDD can be the only manifestation of this systemic disease, with the orbit being the most commonly involved site, exhibiting bone destruction, intracranial and/or sinus involvement and variable degree of visual loss. Ophthalmic familial RDD represent a severe form with a malignant course. Steroid monotherapy may be inadequate to control orbital RDD; thus, combined treatment is usually necessary. A comprehensive approach to assessment and management is recommended.
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页数:8
相关论文
共 37 条
[1]   Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease [J].
Abla, Oussama ;
Jacobsen, Eric ;
Picarsic, Jennifer ;
Krenova, Zdenka ;
Jaffe, Ronald ;
Emile, Jean-Francois ;
Durham, Benjamin H. ;
Braier, Jorge ;
Charlotte, Frederic ;
Donadieu, Jean ;
Cohen-Aubart, Fleur ;
Rodriguez-Galindo, Carlos ;
Allen, Carl ;
Whitlock, James A. ;
Weitzman, Sheila ;
McClain, Kenneth L. ;
Haroche, Julien ;
Diamond, Eli L. .
BLOOD, 2018, 131 (26) :2877-2890
[2]   Rosai-Dorfman disease isolated to the central nervous system: A report of 11 cases [J].
Andriko, JAW ;
Morrison, A ;
Colegial, CH ;
Davis, BJ ;
Jones, RV .
MODERN PATHOLOGY, 2001, 14 (03) :172-178
[3]   LEPTOMENINGEAL AND ORBITAL BENIGN LYMPHOPHAGOCYTIC HISTIOCYTOSIS - CASE-REPORT [J].
ASAI, A ;
MATSUTANI, M ;
KOHNO, T ;
FUJIMAKI, T ;
TANAKA, H ;
KAWAGUCHI, K ;
KOIKE, M ;
TAKAKURA, K .
JOURNAL OF NEUROSURGERY, 1988, 69 (04) :610-612
[4]   ORBITAL SINUS HISTIOCYTOSIS - MR APPEARANCE [J].
BURTON, EM ;
HICKMAN, M ;
BOULDEN, TF ;
JOYNER, RE ;
TIERNEY, MB .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1989, 13 (04) :696-699
[5]   Ophthalmic Findings of Rosai-Dorfman Disease [J].
Choi, Michael B. ;
Salomao, Diva R. ;
Smith, Wendy M. ;
Pulido, Jose S. ;
Garrity, James A. .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2018, 188 :164-172
[6]   A case of orbital Rosai-Dorfman disease responding to radiotherapy [J].
Cooper, Sanutel Lewis ;
Chavis, Pamela S. ;
Fortney, John A. ;
Watkins, John M. ;
Caplan, Michael J. ;
Jenrette, Joseph M., III .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2008, 30 (10) :744-748
[7]  
Destombes P, 1965, Bull Soc Pathol Exot Filiales, V58, P1169
[8]   Histiocytosis [J].
Emile, Jean-Francois ;
Cohen-Aubart, Fleur ;
Collin, Matthew ;
Fraitag, Sylvie ;
Idbaih, Ahmed ;
Abdel-Wahab, Omar ;
Rollins, Barrett J. ;
Donadieu, Jean ;
Haroche, Julien .
LANCET, 2021, 398 (10295) :157-170
[9]  
Emile JF, 2016, BLOOD, V127, P2672, DOI [10.1182/blood-2016-01690636, 10.1182/blood-2016-01-690636]
[10]   OPHTHALMOLOGIC MANIFESTATIONS OF SINUS HISTIOCYTOSIS WITH MASSIVE LYMPHADENOPATHY [J].
FOUCAR, E ;
ROSAI, J ;
DORFMAN, RF .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1979, 87 (03) :354-367