Article Text
PDF
Statistics from Altmetric.com
Description
A previously healthy 54-year-old man presented with gradual vision loss, pain and swelling of the left eye, which started a month prior to admission. He was also experiencing night sweat, mild fever and noticed 10 lb weight loss since symptoms started. Physical examination showed inferior chemosis, lagophthalmos and mild proptosis of the left eye. Head CT showed a left-sided paranasal mass (figure 1), and subsequent MRI demonstrated a large lobulated infiltrative mass centred in the upper left nasal cavity with extension into the left orbits with resultant moderate proptosis and stretching of the optic nerve (figure 2A, B). CT of the chest, abdomen and pelvis revealed no evidence of lymphadenopathy or hepatosplenomegaly. Also, a bone marrow biopsy showed no lymphoid aggregate or interstitial increase of lymphocytes with normal flow cytometry results. A biopsy from the mass confirmed the diagnosis of stage IE extranodal diffuse large B-cell lymphoma (DLBCL) with strong expression of MUM1, CD5, BCL2, CMYC and BCL6, but negative CD3 and CD10 (figures 3A, B and 4A–G), suggesting an aggressive course of disease.1–3 Intravenous prednisone was initiated to minimise optic nerve compression and chemotherapy with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) was started alternating with intravenous methotrexate for central nervous system prophylaxis.4 ,5 The patient completed three courses of R-CHOP, with only partial recovery of visual acuity from 20/200 to 20/100 in a Snellen chart. Paranasal DLBCL is a very rare disease and results in optic nerve compression causing blindness. Prolonged optic nerve compression can lead to irreversible vision loss. Early diagnosis with imaging modalities is pivotal for the prognosis and steroid treatment is essential to minimise the complications from optic nerve compression.
CT of the head. A large infiltrative mass measuring about 47×47×38 mm with mild heterogeneous enhancement is seen centred around the left nasal cavity. This mass is causing destruction of the medial, inferior wall of the left orbit.
(A and B) MRI of the brain. A T1 postcontrast large lobulated infiltrative mass centred in the upper left nasal cavity, with extension into the left orbit with resultant moderate proptosis and stretching of optic nerve, is causing destruction of the left middle turbinate, uncinate process. The mass is extending into the maxillary sinus and also causing erosion and destruction of the cribriform plate, fovea ethmoidalis, wall of frontal sinus and anterior wall of sphenoid sinus on the left side with probable extension into the epidural space and sphenoid sinus.
(A and B) Light microscopic findings evaluation of the biopsy specimens from the paranasal mass at ×100 (A) and ×400 (B) showing neoplastic B-cell proliferation characterised by overall large cell size and centroblastic morphology.
(A–G) Immunohistochemistry staining. The absence of CD3 (A), CD10 (B) with expression of CD5 (C), BCL6 (D), MUM-1 (E) classify this diffuse large B-cell lymphoma as of non-germinal centre origin and activated cell type.3 In addition, these cells express strong BCL2 (F), CMYC (G) and BCL6 (D). These findings suggest triple hit lymphoma with poor prognosis.1 ,2
Learning points
-
Extranodal diffuse large B-cell lymphoma can present with paranasal mass and orbital infiltration in rare cases.
-
Prolonged optic nerve compression by mass can cause irreversible vision loss, and immediate steroid and chemotherapy are essential for a better clinical outcome.
Footnotes
-
Contributors SY, JK and FA were involved in care of the patient, collecting data and all of the authors wrote up the case report. SY reviewed the literature and revised the manuscript.
-
Competing interests None.
-
Patient consent Obtained.
-
Provenance and peer review Not commissioned; externally peer reviewed.