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Year : 2015  |  Volume : 63  |  Issue : 6  |  Page : 555-557

Unicentric Castleman's disease in the orbit: A case report

Department of Ophthalmology, Korea University College of Medicine, Seoul, South Korea

Date of Submission26-Dec-2014
Date of Acceptance02-Jun-2015
Date of Web Publication11-Aug-2015

Correspondence Address:
Dr. Sehyun Baek
Department of Ophthalmology, Guro Hospital, Korea University College of Medicine, 80, Guro-dong, Guro-gu, Seoul, 152-703
South Korea
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0301-4738.162645

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A 53-year-old man presented with a palpable mass on the left lower eyelid and occasional diplopia. Under suspicion of orbital lymphoma, an excisional biopsy was performed, and histopathology revealed Castleman's disease. Castleman's disease is a rare disorder of the lymphoid system, and only a few cases of Castleman's disease in the orbit have been reported.

Keywords: Castleman′s disease, lymphoid system, orbit

How to cite this article:
Kang D, Lee J, Lee H, Baek S. Unicentric Castleman's disease in the orbit: A case report. Indian J Ophthalmol 2015;63:555-7

How to cite this URL:
Kang D, Lee J, Lee H, Baek S. Unicentric Castleman's disease in the orbit: A case report. Indian J Ophthalmol [serial online] 2015 [cited 2020 Jun 5];63:555-7. Available from: http://www.ijo.in/text.asp?2015/63/6/555/162645

Castleman's disease is a rare atypical lymphoproliferative disorder with three histopathological types: Hyaline vascular, plasma cell, and mixed (transitional) cell type. The disease also has two clinical types: Unicentric and multicentric. [1],[2] The mediastinum is the most common site of occurrence and the first reported site by Castleman and Towne in 1954. [3] Intra-orbital involvement of Castleman's disease is rare. This report discusses a hyaline vascular type of Castleman's disease in the orbit.

  Case Report Top

A 53-year-old male presented with a painless, hard, palpable mass around the left lower lid with 4 months duration. On examination, bilateral best corrected visual acuity was 20/20. Under slit lamp examination, mild chemosis was seen on the left bulbar conjunctiva. There was mild eye movement limitation of the lateral downward gaze of the left eye. Hertel exophthalmometric measurements were 19 mm oculus dexter and 21 mm oculus sinister [Figure 1]. During the visit, the patient did not complain of diplopia but described occasional episodes of double vision in the recent past. His medical history was otherwise unremarkable. Computed tomography (CT) scan revealed well enhancing, lobular hyperdense mass in left intraconal space [Figure 2]. With a high clinical and imaging suspicion of lymphoma, an excisional biopsy was performed.
Figure 1: Initial external photograph. Mild chemosis and exophthalmos were seen with the left eye

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Figure 2: Computed tomography revealed a solid, lobular hyperdense mass conforming to the shape of the posterolateral aspect of the left globe in left intraconal space. There were lack of bony involvement, molding around normal structure

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A relatively well circumscribed solid mass [Figure 3] was excised and sent for histological examination. The specimen consisted of a fragment of soft tissue measuring 3.2 cm × 2.6 cm × 1.3 cm. On section, the cut surface appeared whitish and smooth. The sample had a 0.1 cm resection margin. The biopsy showed proliferation of lymphoid follicles with depletion of germinal center lymphocytes and proliferation of dendritic cells and prominent vascularity of the germinal centers. One follicle contained two or more three germinal centers ("twinning") [Figure 4]a-d. Immunohistochemical staining for CD3 and CD20 demonstrated follicular hyperplasia, and CD21 and CD23 staining showed dendritic cell proliferation. The CD5 and cyclin D-1 stains were applied to exclude the possibility of malignant lymphoma, including mantle cell lymphoma. The Ki-67 proliferation marker highlighted some remaining germinal centers. Overall, the mass was revealed to be Castleman's disease of the extranodal, hyaline vascular variant type.
Figure 3: A solid, well-circumscribed, 3.2 cm × 2.6 cm × 1.3 cm solid mass was excised

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Figure 4: (a) Histology of the tissue showed proliferation of lymphoid follicles with depletion of germinal center lymphocytes and proliferation of dendritic cells (H and E, ×200). (b) The "onion-skinning" of mantle zone lymphocytes, together with the prominent central vessel, has been likened to the appearance of a lollipop (H and E, ×400). (c and d) Immunohistochemical stains of CD21 and CD23 demonstrated follicular hyperplasia

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The patient was referred to the Hematology-Oncology Department for systemic workup and treatment. Under the diagnosis of Castleman's disease of the orbit, chest, abdomen and pelvis CT scans were obtained, which were unremarkable. The patient's lab findings (complete blood count, liver function test, lactate dehydrogenase) were normal. The patient is on the 13 months of follow-up till the writing of this report and radiotherapy will be considered if there is recurrence of mass. Follow-up CT scans have been obtained every 3 months, and no specific findings including recurrence of mass have been observed.

  Discussion Top

In 1954, Castleman published a case report that described the eponymous disease for the 1 st time. [3] Castleman's disease within the orbit is extremely rare, the exact incidence unknown, and there have been few reported cases. Until now, only a few cases of Castleman's disease in the orbital area have been published, with the most common being the unicentric, hyaline vascular type. [4],[5],[6],[7],[8]

Histopathologically, Castleman's disease can be classified as a hyaline vascular, plasma cell, or mixed cell type neoplasm, with the hyaline vascular type being the most common. [1],[2] The hyaline vascular type is characterized by hyalinized germinal centers with penetrating blood vessels with surrounding mantle zones of concentric lymphocytes and vascular proliferation of the interfollicular tissue. The plasma cell type is characterized by interfollicular proliferation of plasma cells and is more commonly multicentric than unicentric.

The disease is divided into two clinical subtypes, unicentric and multicentric. The localized type of Castleman's disease commonly presents as the hyaline vascular type. Clinically, most cases present as a solitary mass without other symptoms. [2] Most multicentric Castleman's disease presents histologic features of the plasma cell type. Recently, a few case of the disease most frequently found in immunosuppressed individuals, especially in HIV-positive patients, is described as human herpes virus-8 (HHV-8) associated type. [9]

The multicentric type appears as lesions throughout the body, is commonly associated with fever, chills, night sweats, fatigue and may also accompany lymphadenopathy and organomegaly. The prognosis of this type is usually poor. While the unicentric form can be cured with surgical excision, surgery usually isn't an option for multicentric Castleman's disease because of the number of lymph nodes involved. [7] When treating the multicentric form, treatments such as corticosteroids, chemotherapy, or immunotherapy should be reach all parts of the body. One or a combination of these methods is selected to try and put the disease into remission. [7],[10] Anti-viral drugs including anti-HIV treatment may also be beneficial in the HHV-8 associated type, thus histopathology and immunohistochemistry are important in reaching a diagnosis and exact classification of this rare disease. [9]

The currently described patient had a hyaline vascular type mass with no evidence of other tumor foci or systemic spread, and underwent excisional biopsy. For most unicentric cases, no additional treatment is required. Up to the time of this case report, there has been no evidence of tumor recurrence or other complications. Although relatively rare, ophthalmologists should consider Castleman's disease among the differential diagnoses including lymphoma, hemangioma, and other masses. Understanding the histopathologic and clinical feature of Castleman's disease is important and from an accurate diagnosis, appropriate treatment methods can be selected.

  References Top

Keller AR, Hochholzer L, Castleman B. Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer 1972;29:670-83.  Back to cited text no. 1
Frizzera G. Castleman′s disease and related disorders. Semin Diagn Pathol 1988;5:346-64.  Back to cited text no. 2
Castleman B, Towne VW. Hyperplasia of mediastinal lymph node. N Engl J Med 1954;250:26-30.  Back to cited text no. 3
Jones NW, Fountain TR, Thakral B, Eldibany M. Castleman′s disease in the orbit of a 17-year-old girl: A case report. Ophthal Plast Reconstr Surg 2014;30:e17-20.  Back to cited text no. 4
Park KS, Choi YJ, Song KS. Hyaline-vascular type Castleman′s disease involving both orbits. Acta Ophthalmol Scand 2002;80:537-9.  Back to cited text no. 5
Alyahya GA, Prause JU, Heegaard S. Castleman′s disease in the orbit. A 20-year follow-up. Acta Ophthalmol Scand 2002;80:540-2.  Back to cited text no. 6
Bowne WB, Lewis JJ, Filippa DA, Niesvizky R, Brooks AD, Burt ME, et al. The management of unicentric and multicentric Castleman′s disease: A report of 16 cases and a review of the literature. Cancer 1999;85:706-17.  Back to cited text no. 7
Kurokawa T, Suzuki S, Kawaguchi K, Fujisawa N, Yoshimura N. Castleman disease presenting with ophthalmic signs and symptoms. Am J Ophthalmol 1999;128:114-6.  Back to cited text no. 8
Cronin DM, Warnke RA. Castleman disease: An update on classification and the spectrum of associated lesions. Adv Anat Pathol 2009;16:236-46.  Back to cited text no. 9
Gittinger JW Jr. Ocular involvement in Castleman′s disease. Response to radiotherapy. Ophthalmology 1989;96:1646-9.  Back to cited text no. 10


  [Figure 1], [Figure 2], [Figure 3], [Figure 4]


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