The 20 references with contexts in paper X. Yang, S. Gvetadze R., K. Ilkaev D., M. Lv, J. Sun, J. Li, C. Ян, Ш. Гветадзе Р., К. Илькаев Д., М. Лю, Дж. Суэн, Дж. Ли (2018) “Экстранодальная интраоссальная болезнь Розаи–Дорфмана в области нижней челюсти: описание клинического случая и обзор литературы // Extranodal intraosseous Rosai–Dorfman disease in the lower jaw: a case report and review of the literature” / spz:neicon:ogsh:y:2018:i:2:p:34-38

1
Rosai J., Dorfman R. F. Sinus histiocytosis with massive lymphadenopathy: a newly recognized benign clinicopathologic entity. Arch Pathol 1969;87:63–70.
Total in-text references: 1
  1. In-text reference with the coordinate start=4478
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    Introduction Rosai–Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy was first described by P. Destombes in 1965 and further deeply researched by J. Rosai and R. F. Dorfman
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    [1, 2]
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    . In most cases this benign condition manifests with pseudolymphomatous proliferation of the sinusoidal histiocytes in the regional lymph nodes. Cervical lymph nodes are most commonly involved though numerous cases of mediastinal, axillary, inguinal and retroperitoneal nodal group disease were reported [3].

2
Rosai J., Dorfman R. F. Sinus histiocytosis with massive lymphadenopathy: a pseudolymphomatous benign disorder. Analysis of 34 cases. Cancer 1972;30(5):1174–88. PMID: 5083057.
Total in-text references: 1
  1. In-text reference with the coordinate start=4478
    Prefix
    Introduction Rosai–Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy was first described by P. Destombes in 1965 and further deeply researched by J. Rosai and R. F. Dorfman
    Exact
    [1, 2]
    Suffix
    . In most cases this benign condition manifests with pseudolymphomatous proliferation of the sinusoidal histiocytes in the regional lymph nodes. Cervical lymph nodes are most commonly involved though numerous cases of mediastinal, axillary, inguinal and retroperitoneal nodal group disease were reported [3].

3
Suster S., Cartagena N., CabelloInchausti B., Robinson M. J. Histiocytic lymphophagocytic panniculitis. An unusual extranodal presentation of sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease). Arch Dermatol 1988;124(8):1246–9. PMID: 3401030.
Total in-text references: 1
  1. In-text reference with the coordinate start=4790
    Prefix
    In most cases this benign condition manifests with pseudolymphomatous proliferation of the sinusoidal histiocytes in the regional lymph nodes. Cervical lymph nodes are most commonly involved though numerous cases of mediastinal, axillary, inguinal and retroperitoneal nodal group disease were reported
    Exact
    [3]
    Suffix
    . Clinically in most cases this leads to bilateral, painless lymphadenopathy which may be anticipated by febrile incidents with elevated white blood counts. Extranodal lesions are observed in 45 % of the affected subjects [4].

4
Wenig B. M., Abbondanzo S. L., Childers E. L. et al. Extranodal sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) of the head and neck. Hum Pathol 1993;24(5):483–92. PMID: 8491488.
Total in-text references: 2
  1. In-text reference with the coordinate start=5016
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    Clinically in most cases this leads to bilateral, painless lymphadenopathy which may be anticipated by febrile incidents with elevated white blood counts. Extranodal lesions are observed in 45 % of the affected subjects
    Exact
    [4]
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    . These extranodal cases are not associated with lymphadenopathy and may present with several locations concomitantly or as solitary lesions. Among extranodal sites most familiar are the digestive tract, upper airways, orbit, skin and long bones [5–7].

  2. In-text reference with the coordinate start=10687
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    Teeth vitality in the affected area is maintained though the growing mass can to provoke dental mobility and/or root resorption. A small number of cases describing mandible involvement are available
    Exact
    [4, 11–13]
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    . Of these only 1 patient presented with a generalized RDD form with bilateral cervical, axillary and inguinal lymphadenopathy, and local intraosseous RDD of the maxillary, mandible and zygomatic bones [11].

5
Aoyama K., Terashima K., Imai Y. et al. Sinus histiocytosis with massive lymphadenopathy. A histogenic analysis of histiocytes found in the fourth Japanese case. Acta Pathol Jpn 1983;34(2):375–88. PMID: 6741550.
Total in-text references: 1
  1. In-text reference with the coordinate start=5265
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    These extranodal cases are not associated with lymphadenopathy and may present with several locations concomitantly or as solitary lesions. Among extranodal sites most familiar are the digestive tract, upper airways, orbit, skin and long bones
    Exact
    [5–7]
    Suffix
    . Definitive diagnosis is established with pathological and immunohistochemistry exam. In the present paper we describe a patient, who presented with complaints about unilateral sensory deficiency in the area of mental nerve innervation and proved to bear intraosseous Rosai–Dorfman disease of the mandible.

6
Hamels J., Fiasse L., Thiery J. Atypical lymphohistiocytic bone tumour (osseous variant of Rosai–Dorfman disease?). Virchows Arch A Pathol Anat Histopathol 1985;408(2–3):183–9. PMID: 3936259.
Total in-text references: 2
  1. In-text reference with the coordinate start=5265
    Prefix
    These extranodal cases are not associated with lymphadenopathy and may present with several locations concomitantly or as solitary lesions. Among extranodal sites most familiar are the digestive tract, upper airways, orbit, skin and long bones
    Exact
    [5–7]
    Suffix
    . Definitive diagnosis is established with pathological and immunohistochemistry exam. In the present paper we describe a patient, who presented with complaints about unilateral sensory deficiency in the area of mental nerve innervation and proved to bear intraosseous Rosai–Dorfman disease of the mandible.

  2. In-text reference with the coordinate start=11123
    Prefix
    Radiologic features of RDD bone involvement are heterogeneous and range from well-outlined regularly bordered conglomerates to infiltrative lesions with ill-defined borders with or without periosteal spicule reaction
    Exact
    [6, 7, 14]
    Suffix
    . Microscopic and immunohistochemical analysis remains the pillar of RDD diagnosis. One characteristic morphologic finding of the disorder is emperipolesis. As defined by J. G. Humble et al. (1956) emperipolesis is “the active penetration of one cell by another which remains intact” [15].

7
Pendse A. A., Wobker S. E., Greene K. G. et al. Intraosseous Rosai–Dorfman disease diagnosed by touch imprint cytology evaluation: a case series. Diagn Cytopathol 2018;46(1):83–7. DOI: 10.1002/dc.23802. PMID: 28834636.
Total in-text references: 4
  1. In-text reference with the coordinate start=5265
    Prefix
    These extranodal cases are not associated with lymphadenopathy and may present with several locations concomitantly or as solitary lesions. Among extranodal sites most familiar are the digestive tract, upper airways, orbit, skin and long bones
    Exact
    [5–7]
    Suffix
    . Definitive diagnosis is established with pathological and immunohistochemistry exam. In the present paper we describe a patient, who presented with complaints about unilateral sensory deficiency in the area of mental nerve innervation and proved to bear intraosseous Rosai–Dorfman disease of the mandible.

  2. In-text reference with the coordinate start=9656
    Prefix
    Subsequently after first presentations it became evident that this process may evolve in extranodal location with no associated lymphadenopathy. Osseous structures are seldom affected and more commonly lesions of long bones are described
    Exact
    [7]
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    . More than 70 % of the extranodal RDD are seen in the head and neck region [8]. Facial bones affection rate is reported to be low, being less than 8 % of all cases [9, 10]. When considering manifestation of the RDD the symptoms can be clearly divided into general and local.

  3. In-text reference with the coordinate start=11123
    Prefix
    Radiologic features of RDD bone involvement are heterogeneous and range from well-outlined regularly bordered conglomerates to infiltrative lesions with ill-defined borders with or without periosteal spicule reaction
    Exact
    [6, 7, 14]
    Suffix
    . Microscopic and immunohistochemical analysis remains the pillar of RDD diagnosis. One characteristic morphologic finding of the disorder is emperipolesis. As defined by J. G. Humble et al. (1956) emperipolesis is “the active penetration of one cell by another which remains intact” [15].

  4. In-text reference with the coordinate start=11915
    Prefix
    Immunohistochemistry exhibits qualities of antigen presenting cell or Langerhans cell (S-100 positive) and phagocytic histiocytes (α1-antitrypsin, lysozymes, CD-68, MAC-378 positivity and CD-1a negativity) [16]. Recently touch imprint cytology was suggested as a reliable diagnostic alternative for an open excisional biopsy technique for intraosseous RDD
    Exact
    [7]
    Suffix
    . Extranodal intraosseous RDD may be considered fairly rare entity in the maxillofacial region. Several descriptions of facial bone involvement can be found in the literature, more often orbital and sinus disease is reported.

8
Naidu R. K., Urken M. L., Som P. M. et al. Extranodal head and neck sinus histiocytosis with massive lymphadenopathy. Otolaryngol Head Neck Surg 1990;102(6):764–7.
Total in-text references: 1
  1. In-text reference with the coordinate start=9730
    Prefix
    Subsequently after first presentations it became evident that this process may evolve in extranodal location with no associated lymphadenopathy. Osseous structures are seldom affected and more commonly lesions of long bones are described [7]. More than 70 % of the extranodal RDD are seen in the head and neck region
    Exact
    [8]
    Suffix
    . Facial bones affection rate is reported to be low, being less than 8 % of all cases [9, 10]. When considering manifestation of the RDD the symptoms can be clearly divided into general and local. General symptoms (pyrexia, weight loss, leukocytosis, high erythrocyte sedimentation rate) are commonly exhibited in the classic form of RDD with lymphadenopathy.

9
Foucar E., Rosai J., Dorfman R. F. Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease): review of the entity. Semin Diagn Pathol 1990;7(1):19–73. PMID: 2180012.
Total in-text references: 1
  1. In-text reference with the coordinate start=9819
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    Osseous structures are seldom affected and more commonly lesions of long bones are described [7]. More than 70 % of the extranodal RDD are seen in the head and neck region [8]. Facial bones affection rate is reported to be low, being less than 8 % of all cases
    Exact
    [9, 10]
    Suffix
    . When considering manifestation of the RDD the symptoms can be clearly divided into general and local. General symptoms (pyrexia, weight loss, leukocytosis, high erythrocyte sedimentation rate) are commonly exhibited in the classic form of RDD with lymphadenopathy.

10
Carbone A., Passannante A., Gloghini A. et al. A review of sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) of head and neck. Ann Otol Rhinol Laryngol 1999;108(11 Pt 1):1095–104. DOI: 10.1177/000348949910801113. PMID: 10579239.
Total in-text references: 1
  1. In-text reference with the coordinate start=9819
    Prefix
    Osseous structures are seldom affected and more commonly lesions of long bones are described [7]. More than 70 % of the extranodal RDD are seen in the head and neck region [8]. Facial bones affection rate is reported to be low, being less than 8 % of all cases
    Exact
    [9, 10]
    Suffix
    . When considering manifestation of the RDD the symptoms can be clearly divided into general and local. General symptoms (pyrexia, weight loss, leukocytosis, high erythrocyte sedimentation rate) are commonly exhibited in the classic form of RDD with lymphadenopathy.

11
Günhan O., Finci R., Günaydin Y., Somuncu I. Sinus histiocytosis with massive lymphadenopathy: a case with facial bones involvement. J Oral Maxillofac Surg 1991;49(2):205–9. PMID: 1990100.
Total in-text references: 2
  1. In-text reference with the coordinate start=10687
    Prefix
    Teeth vitality in the affected area is maintained though the growing mass can to provoke dental mobility and/or root resorption. A small number of cases describing mandible involvement are available
    Exact
    [4, 11–13]
    Suffix
    . Of these only 1 patient presented with a generalized RDD form with bilateral cervical, axillary and inguinal lymphadenopathy, and local intraosseous RDD of the maxillary, mandible and zygomatic bones [11].

  2. In-text reference with the coordinate start=10899
    Prefix
    Of these only 1 patient presented with a generalized RDD form with bilateral cervical, axillary and inguinal lymphadenopathy, and local intraosseous RDD of the maxillary, mandible and zygomatic bones
    Exact
    [11]
    Suffix
    . Radiologic features of RDD bone involvement are heterogeneous and range from well-outlined regularly bordered conglomerates to infiltrative lesions with ill-defined borders with or without periosteal spicule reaction [6, 7, 14].

12
Alawi F., Robinson B. T., Carrasco L. Rosai–Dorfman disease of the mandible. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006;102(4):506–12. DOI: 10.1016/j.tripleo.2005.10.071. PMID: 16997119.
Total in-text references: 1
  1. In-text reference with the coordinate start=10687
    Prefix
    Teeth vitality in the affected area is maintained though the growing mass can to provoke dental mobility and/or root resorption. A small number of cases describing mandible involvement are available
    Exact
    [4, 11–13]
    Suffix
    . Of these only 1 patient presented with a generalized RDD form with bilateral cervical, axillary and inguinal lymphadenopathy, and local intraosseous RDD of the maxillary, mandible and zygomatic bones [11].

13
Tekin U., Tüz H. H., Günhan O. Reconstruction of a patient with Rosai– Dorfman disease using ramus graft and osseointegrated implants: a case report. J Oral Implantol 2012;38(1):79–83. DOI: 10.1563/AAID-JOI–D-10-00056.1. PMID: 20553156.
Total in-text references: 1
  1. In-text reference with the coordinate start=10687
    Prefix
    Teeth vitality in the affected area is maintained though the growing mass can to provoke dental mobility and/or root resorption. A small number of cases describing mandible involvement are available
    Exact
    [4, 11–13]
    Suffix
    . Of these only 1 patient presented with a generalized RDD form with bilateral cervical, axillary and inguinal lymphadenopathy, and local intraosseous RDD of the maxillary, mandible and zygomatic bones [11].

14
Xu Q., Fu L., Liu C. Multimodality imaging-based evaluation of Rosai– Dorfman disease in the head and neck: a retrospective observational study. Medicine (Baltimore) 2017;96(51):e9372. DOI: 10.1097/MD.0000000000009372. PMID: 29390533.
Total in-text references: 1
  1. In-text reference with the coordinate start=11123
    Prefix
    Radiologic features of RDD bone involvement are heterogeneous and range from well-outlined regularly bordered conglomerates to infiltrative lesions with ill-defined borders with or without periosteal spicule reaction
    Exact
    [6, 7, 14]
    Suffix
    . Microscopic and immunohistochemical analysis remains the pillar of RDD diagnosis. One characteristic morphologic finding of the disorder is emperipolesis. As defined by J. G. Humble et al. (1956) emperipolesis is “the active penetration of one cell by another which remains intact” [15].

15
Humble J. G., Jayne W. H., Pulvertaft R. J. Biological interaction between lymphocytes and other cells. Br J Haematol 1956;2(3):283–94. PMID: 13342362.
Total in-text references: 1
  1. In-text reference with the coordinate start=11418
    Prefix
    One characteristic morphologic finding of the disorder is emperipolesis. As defined by J. G. Humble et al. (1956) emperipolesis is “the active penetration of one cell by another which remains intact”
    Exact
    [15]
    Suffix
    . In RDD histiocytes have a round nuclei with distinct nucleoli and abundant amphophilic to eosinophilic granular or clear cytoplasm. Immunohistochemistry exhibits qualities of antigen presenting cell or Langerhans cell (S-100 positive) and phagocytic histiocytes (α1-antitrypsin, lysozymes, CD-68, MAC-378 positivity and CD-1a negativity) [16].

16
Rastogi V., Sharma R., Misra S. R. et al. Emperipolesis – a review. J Clin Diagn Res 2014;8(12):ZM01–2. DOI: 10.7860/JCDR/2014/10361.5299. PMID: 25654060.
Total in-text references: 1
  1. In-text reference with the coordinate start=11764
    Prefix
    Immunohistochemistry exhibits qualities of antigen presenting cell or Langerhans cell (S-100 positive) and phagocytic histiocytes (α1-antitrypsin, lysozymes, CD-68, MAC-378 positivity and CD-1a negativity)
    Exact
    [16]
    Suffix
    . Recently touch imprint cytology was suggested as a reliable diagnostic alternative for an open excisional biopsy technique for intraosseous RDD [7]. Extranodal intraosseous RDD may be considered fairly rare entity in the maxillofacial region.

17
Smith R. M., Hassan A., Robertson C. E. Numb chin syndrome. Curr Pain Headache Rep 2015;19(9):44. DOI: 10.1007/s11916-015-0515-y. PMID: 26210355.
Total in-text references: 1
  1. In-text reference with the coordinate start=14129
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    The so called dumb chin syndrome was the first and the only manifestation of the intraosseous mandibular RDD as in most of the reported lower jaw involvements. This suggests that RDD is another lymphoproliferative neoplasia which should be included in the differential diagnosis of the dumb chin syndrome
    Exact
    [17]
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    . Treatment strategies which are advocated in the literature tend to depend on the form of the disease. Corticosteroid-based schemes are currently prescribed and are reported to be effective in cases of nodal RDD or extranodal disease without bone involvement [18].

18
Lai K. L., Abdullah V., Ng K. S. et al. Rosai–Dorfman disease: presentation, diagnosis, and treatment. Head Neck 2013;35(3):E85–8. DOI: 10.1002/ hed.21930. PMID: 22083607.
Total in-text references: 1
  1. In-text reference with the coordinate start=14395
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    Treatment strategies which are advocated in the literature tend to depend on the form of the disease. Corticosteroid-based schemes are currently prescribed and are reported to be effective in cases of nodal RDD or extranodal disease without bone involvement
    Exact
    [18]
    Suffix
    . Exceptional observations of steroid-resistant extranodal soft-tissue RDD were shown to benefit from radiotherapy [19]. On the other hand, surgical management either in form of conservative curettage or radical resection is generally chosen for intraosseous RDD.

19
Maklad A. M., Bayoumi Y., Tunio M. et al. Steroid-resistant extranodal Rosai– Dorfman disease of the cheek mass and ptosis treated with radiation therapy. Case Rep Hematol 2013;2013:428297. DOI: 10.1155/2013/428297. PMID: 23738161.
Total in-text references: 1
  1. In-text reference with the coordinate start=14514
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    Corticosteroid-based schemes are currently prescribed and are reported to be effective in cases of nodal RDD or extranodal disease without bone involvement [18]. Exceptional observations of steroid-resistant extranodal soft-tissue RDD were shown to benefit from radiotherapy
    Exact
    [19]
    Suffix
    . On the other hand, surgical management either in form of conservative curettage or radical resection is generally chosen for intraosseous RDD. If performed properly surgical treatment assures excellent prognosis though cases of recurrences were outlined [20].

20
Shemen L., D’Anton M., Klijian A. et al. Rosai–Dorfman disease involving the premaxilla. Ann Otol Rhinol Laryngol 1991;100(10):845–51. DOI: 10.1177/000348949110001011.
Total in-text references: 1
  1. In-text reference with the coordinate start=14776
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    On the other hand, surgical management either in form of conservative curettage or radical resection is generally chosen for intraosseous RDD. If performed properly surgical treatment assures excellent prognosis though cases of recurrences were outlined
    Exact
    [20]
    Suffix
    .