[Home ] [Archive]   [ فارسی ]  
:: Volume 24, Issue 1 (Iranian Journal of Ophthalmology 2012) ::
2012, 24(1): 83-83 Back to browse issues page
Letter to the Editor: Author reply
Yungang Ding Dr., Yi Du Dr., Hehua Ye Dr., Huijing Ye Dr., Huasheng Yang Dr. *
, yanghs64@126.com
Abstract:   (5706 Views)

  Dear Editor:

  We thank Dr Asadi Amoli for her interest in our article. 1 Dr Asadi Amoli pointed out that specific and sensitive rhabdomyosarcoma (RMS) markers should be investigated in our case. 2 We agree with Dr Asadi Amoli ’s opinion and are sorry that the results of pathology examination and myogenin (myf-4) staining studied in a local hospital were not provided in our case report.

  An excisional biopsy in our case was performed by local ophthalmologists, and myogenin staining by the local pathologists was positive for tumor cells (figure 1 A). When the patient was referred to Zhongshan Ophthalmic Center, our pathologists reviewed the pathology examination, and the patient was diagnosed as conjunctival RMS. After surgery in our center, histopathologic examination showed the RMS cells staining for markers of desmin, muscle-specific actin and vimentin.

  In our case , tumor was mostly composed of primitive round and spindle cells (figure 1 B) and scattered cells acquired abundant cytoplasmic eosinophilia and elongate shapes (figure 1 C), all of which were consistent with features of RMS. 3,4

  It is indicated that immunochemical staining provided further support for the histogenesis and diagnosis of RMS. Only vimentin is present in the most primitive cells. Desmin and actin are acquired by developing rhabdomyoblasts, and differentiated cells express myoglobin which is specific for striated muscle. 3 Nevertheless, myoglobin was not highly sensitive to RMS. Positive immunostaining for nuclear MyoD and myogenin is found to be highly specific and sensitive to RMS. 3,5 In our case, vimentin, desmin, muscle-specific actin and myogenin, all of which were positive in our case, provided further support for the histogenesis and diagnosis of RMS.

 

 

  References

 

  1. Ye H, Ye H, Ding Y, et al. Primary conjunctival rhabdomyosarcoma successfully treated with surgery and chemotherapy. Iranian Journal of Ophthalmology 201123(4):65-8.

  2. Asadi Amoli F. Commentary on immunohistochemical diagnosis of rhabdomyosarcoma. Iranian Journal of Ophthalmology 201224(1):82.

  3. Parham DM, Barr FG. Embryonal rhabdomyosarcoma. In: Fletcher CDM, Unni KK, Mertens F, eds. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Lyon: IARC Press’ 2002146-9.

  4. Shields JA, Shields CL. Rhabdomyosarcoma: review for the ophthalmologist. Surv Ophthalmol 200348(1):39-57.

  5. Demirci H, Elner VM. Tumors of soft tissue. In: Klintworth GK, Garner A, eds. Garner and Klintworth's pathobiology of ocular disease. 3 ed. New York: Informa Healthcare USA’ 20081383-7.

 

 

Keywords: -
Full-Text [PDF 125 kb]   (1738 Downloads)    
Type of Study: General | Subject: General
Send email to the article author

Add your comments about this article
Your username or Email:

Write the security code in the box >


XML     Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ding Y, Du Y, Ye H, Ye H, Yang H. Letter to the Editor: Author reply. Iranian Journal of Ophthalmology. 2012; 24 (1) :83-83
URL: http://irjo.org/article-1-615-en.html


Volume 24, Issue 1 (Iranian Journal of Ophthalmology 2012) Back to browse issues page
مجله چشم پزشکی ایران Iranian Journal of Ophthalmology
Persian site map - English site map - Created in 0.05 seconds with 30 queries by YEKTAWEB 3638