scholarly journals A Case of Primary Non-Hodgkin’s Lymphoma of the External Auditory Canal

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Luca Bruschini ◽  
Andrea De Vito ◽  
Susanna Fortunato ◽  
Marco Pelosini ◽  
Giulia Cervetti ◽  
...  

Lymphomas represent the second most frequent malignant tumor (incidence 2.5%) in the head and neck region. Non-Hodgkin lymphomas (NHLs) present with cervical lymph node involvement, but in 40% extranodal site could be primary involved: nasopharynx, the lacrimal sac, the temporal bone, or the others areas. NHLs of the ear are rarely reported. In this report, we described a patient with primary NHL of the external ear canal who was successfully treated with surgical excision and chemotherapy.

2005 ◽  
Vol 446 (5) ◽  
pp. 546-554 ◽  
Author(s):  
Ömer Uluoğlu ◽  
Nalan Akyürek ◽  
Aytuğ Üner ◽  
Uğur Coşkun ◽  
Ayşegul Özdemir ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
A. Bahar Ceyran ◽  
Serkan Şenol ◽  
Barış Bayraktar ◽  
Şeyma Özkanlı ◽  
Z. Leyla Cinel ◽  
...  

A 37-year-old male case was admitted with goiter. Ultrasonography of thyroid showed a 5 cm cystic nodule in the left lobe with a 1.5 cm solid component. Fine needle aspiration biopsy revealed atypia of undetermined significance or follicular lesion. The patient was operated on. The pathological diagnosis was reported as papillary thyroid carcinoma. The immunohistochemical examination showed multiple foci of Langerhans cell histiocytosis involving both lobes. The patient died due to cardiac arrest with respiratory causes in the early postoperative period. Langerhans cell histiocytosis is a rare primary condition which involves abnormal clonal proliferation of Langerhans cells in various tissues and organs. Thyroid involvement is infrequently seen. Although the etiology is unknown, genetic components may be linked to the disease. It is also associated with a family history of thyroid disease. Papillary thyroid carcinoma is the most common malignant epithelial tumor of the thyroid gland. Langerhans cell histiocytosis presenting with papillary thyroid carcinoma is rare. The privilege of our case is langerhans cell histiocytosis of the thyroid with multiple cervical lymph node involvement accompanying cervical lymph node metastatic thyroid papillary carcinoma.


Cancer ◽  
2009 ◽  
Vol 115 (7) ◽  
pp. 1489-1497 ◽  
Author(s):  
Shao Hui Huang ◽  
David Hwang ◽  
Gina Lockwood ◽  
David P. Goldstein ◽  
Brian O'Sullivan

2011 ◽  
Vol 38 (6) ◽  
pp. 710-717 ◽  
Author(s):  
Masanobu Taniguchi ◽  
Akihito Watanabe ◽  
Hitoshi Tsujie ◽  
Takayo Tomiyama ◽  
Masahiro Fujita ◽  
...  

2013 ◽  
Vol 127 (S2) ◽  
pp. S17-S23 ◽  
Author(s):  
M S Elliott ◽  
K Gao ◽  
R Gupta ◽  
E L Chua ◽  
A Gargya ◽  
...  

AbstractBackground:The incidence of papillary thyroid cancer is rising, with an increase in the number of microcarcinomas being discovered. There is controversy in the literature regarding the optimal management of these tumours. This study aimed to review our institution's experience with the presentation and management of papillary thyroid microcarcinoma.Methods:Retrospective analysis from the Sydney Head and Neck Cancer Institute, from 1987 to 2009.Results:A total of 228 patients were analysed. Papillary thyroid microcarcinomas were discovered incidentally in 116 (50.9 per cent) patients and non-incidentally in the remaining 112 (49.1 per cent) patients. Amongst the non-incidental group, 11.6 per cent of patients presented with lateral cervical lymph node involvement. Non-incidental microcarcinomas were significantly associated with younger age (<45 years) (p = 0.007) and larger tumours (5–10 mm) (p < 0.001). Only four patients in the incidental group suffered recurrent disease (locoregional). No patient developed distant metastatic disease or died during follow up.Conclusion:Papillary thyroid microcarcinomas present both incidentally and non-incidentally, with equal prevalence. Non-incidental tumours not infrequently present with cervical lymph node disease. The patient outcome is generally excellent.


Sign in / Sign up

Export Citation Format

Share Document