scholarly journals Masquerading solitary plasmacytoma; an eyelid lump in disguise

2021 ◽  
Vol 14 (1) ◽  
pp. 42
Author(s):  
Aleza Andron ◽  
Uri Peleg ◽  
Chezi Genzel ◽  
Elena Drabkin
2005 ◽  
Vol 174 (1) ◽  
pp. 33-36
Author(s):  
H. S. Coskun ◽  
O. Er ◽  
S. Soyuer ◽  
M. Altinbas ◽  
B. Eser ◽  
...  

Author(s):  
Deborah A. Frassica ◽  
Frank J. Frassica ◽  
Mark F. Schray ◽  
Franklin H. Sim ◽  
Robert A. Kyle

2003 ◽  
Vol 10 (2) ◽  
pp. 266-268 ◽  
Author(s):  
Ertugrul Çakir ◽  
Gökalp Karaarslan ◽  
Haydar Usul ◽  
Süleyman Baykal ◽  
Erhan Arslan

2010 ◽  
Vol 14 (2) ◽  
pp. 149-152 ◽  
Author(s):  
Debra Rattican ◽  
Debra L. Kelly ◽  
Kristin A. Filler ◽  
Debra E. Lyon

2021 ◽  
Vol 21 ◽  
pp. S256
Author(s):  
Zhanna Kozich ◽  
Victor Martinkov ◽  
Janna Pugacheva ◽  
Michail Zhandarov ◽  
Liudmila Smirnova

Spinal Cord ◽  
1998 ◽  
Vol 36 (7) ◽  
pp. 470-475 ◽  
Author(s):  
Hisatoshi Baba ◽  
Yasuhisa Maezawa ◽  
Nobuaki Furusawa ◽  
Makoto Wada ◽  
Yasuo Kokubo ◽  
...  

FACE ◽  
2021 ◽  
pp. 273250162110536
Author(s):  
Joshua Harrison ◽  
Samantha Marley ◽  
Shawhin Shahriari ◽  
Christian Bowers ◽  
Anil Shetty

We report a rare case of an extramedullary plasmacytoma (EMP) in the frontal sinus with an indolent clinical presentation. Although a history of trauma was absent, the initial diagnosis was a mucocele, based on the radiological findings. Upon surgical excision, the patient was found to have an EMP. EMP, a form of solitary plasmacytoma, has a significantly high rate of conversion to multiple myeloma. This mandates long-term follow-up, even after successful radiotherapy and/or resection. While radiation therapy is generally considered a first line treatment for EMP, surgical intervention may provide optimal treatment in complicated cases. This case presentation highlights the prognosis of patients diagnosed with EMP.


2021 ◽  
Vol 4 (5) ◽  
pp. 01-04
Author(s):  
Salma Fares ◽  
Adil Taoufik ◽  
Aissam Maataoui ◽  
Kaoutar Sokori ◽  
Ouadie Qamouss

Background: Solitary plasmacytoma is a rare malignant neoplasm of plasma cells accounting 5-10% of all plasma cell dyscrasias with extramedullary plasmocytoma in 3- 5%. Their localization in the female genital tract is quite rare, either as solitary plasmacytomas or as part of a disseminated MM. Solitary ovarian plasmocytoma is extremely rare. Case: A 52-year-old woman, presented presented postmenopausal recurring episodes of metrorrhagia with left ovarian mass. She was diagnosed with solitary ovarianplasmocytoma without systemicdisease. The patient underwent complete surgery resection and a full work up to rule out multiple myeloma that objectived a small serum monoclonal protein that had resolved postoperatively. At 17 months of follow-up, the patient is still alive and doing well with no signs of recurrence or progression to mutliple myeloma. Although rare, solitary plasmacytoma of the ovary can occur without any overt symptoms or laboratory abnormalities tests and require prompt and adequate treatment and rigorous monitoring due to their ability to relapse or progress to MM. Complete surgical resection followed by activesurveillance is appropriate.


Sign in / Sign up

Export Citation Format

Share Document