Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 2930
  • Home
  • Print this page
  • Email this page

   Table of Contents      
ONE MINUTE OPHTHALMOLOGY
Year : 2020  |  Volume : 68  |  Issue : 4  |  Page : 554

Bilateral lacrimal sac swellings in the elderly: Not always a mucocele


1 Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India
2 Department of Ophthalmology, Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab, India

Date of Web Publication16-Mar-2020

Correspondence Address:
Dr. Shakeen Singh
Department of Ophthalmology, Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_1490_19

Rights and Permissions

How to cite this article:
Singh M, Kaur M, Singh S. Bilateral lacrimal sac swellings in the elderly: Not always a mucocele. Indian J Ophthalmol 2020;68:554

How to cite this URL:
Singh M, Kaur M, Singh S. Bilateral lacrimal sac swellings in the elderly: Not always a mucocele. Indian J Ophthalmol [serial online] 2020 [cited 2020 Jun 4];68:554. Available from: http://www.ijo.in/text.asp?2020/68/4/554/280710



A 62-year-male, hypertensive, had a 6-month history of painless, progressive bilateral (OU) lacrimal sac region swellings without epiphora. Examination revealed pea-sized swelling over the lacrimal sac regions OU (left eye > right eye) [Figure 1]a. On syringing and irrigation, lacrimal system was freely patent. A detailed evaluation revealed inferior dystopia of the right eye (OD), and pinkish-red, lobulated, subconjunctival mass with vascularization was noted in the right superior and left inferior fornices [Figure 1]a. The rest of ophthalmic examination was normal. MRI orbits revealed similar soft-tissue lesions in both orbits, lacrimal sacs, and nasolacrimal ducts (NLD) [Fig. 1b]. Lacrimal sac fine needle aspiration cytology (FNAC) [Fig. 1c], and orbitotomy-incision biopsy [[Figure 1]d suggested a low-grade non-Hodgkin's mucosa-associated lymphoid tissue (MALT) lymphoma (predominant CD20+).
Figure 1:(a) Bilateral lacrimal sac region swellings (white arrows), right inferior dystopia, and left inferior orbital sulcus fullness. (b) MRI orbits (axial T2-weighted) shows bilateral lacrimal sac wall thickening (white arrows) and iso-intense orbital masses (arrowheads). (c) Cytology (10×) shows small round blue cells with coarse chromatin and scanty cytoplasm. (d) Sheets of round blue cells suggestive of lymphomatous malignancy (10×, H and E). (e) After chemotherapy, bilateral lacrimal sac regions and the right eye appears normal

Click here to view



  What is Your Next Step? Top


  1. Orbitotomy and excision biopsy + dacryocystorhinostomy
  2. Orbitotomy and excision biopsy + dacryocystectomy
  3. Systemic workup + orbitotomy and mass excision + dacryocystorhinostomy
  4. Systemic workup followed by chemotherapy ± radiotherapy.



  Correct Answer: D Top



  Findings Top


The systemic workup revealed splenomegaly, enlarged para-aortic lymph nodes, and bone marrow infiltration with lymphomatous cells. Systemic chemotherapy was advised by the hemato-oncology department, including cyclophosphamide, doxorubicin, vincristine, and prednisolone. After the 6th cycle, the patient showed complete resolution of both orbital and lacrimal sac region masses [Fig. 1e]. Radiotherapy was deferred due to complete resolution post-chemotherapy. The patient was alive and disease-free locally, and systemically at 2 years follow-up recently.


  Diagnosis Top


Bilateral lacrimal sac and orbital non-Hodgkin's MALT lymphoma.


  Discussion Top


The MALT lymphomas are common among all lacrimal sac lymphomas (LSL).[1] The diffuse large B-cell lymphoma behaves more aggressively, hence, have a poorer prognosis.[1],[2] Among Japanese, 50% of LSL is of diffuse B-cell type while in western literature, the MALT lymphoma is reported to be more common (33%).[2]

The majority of LSL patients do not have epiphora due to the patent lumen of NLD as the lymphoma cells infiltrate the lacrimal drainage system associated lymphoid tissue (LDALT).[1],[2],[3] The lack of prominent symptoms may lead to delayed presentation and diagnosis of LSL. MRI provides adequate information for orbital-adnexal lymphomas.[1],[2],[3] Chemotherapy provides a successful outcome in terms of both local and systemic disease control.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Singh S, Ali MJ. Lymphoproliferative tumors involving the lacrimal drainage system: A major review. Orbit 2019;3:1-9.  Back to cited text no. 1
    
2.
Sabundayo MS, Takahashi Y, Kakizaki H. Lacrimal sac lymphoma: A series of Japanese patients. Eur J Ophthalmol 2019;29:678-84.  Back to cited text no. 2
    
3.
Sjö LD, Ralfkiaer E, Juhl BR, Prause JU, Kivelä T, Auw-Haedrich C, et al. Primary lymphoma of the lacrimal sac: An EORTC ophthalmic oncology task force study. Br J Ophthalmol 2006;90:1004-9.  Back to cited text no. 3
    


    Figures

  [Figure 1]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
What is Your Nex...
Correct Answer: D
Findings
Diagnosis
Discussion
References
Article Figures

 Article Access Statistics
    Viewed1225    
    Printed19    
    Emailed0    
    PDF Downloaded336    
    Comments [Add]    

Recommend this journal