Azygos vein diverticulum, a rare case of a mediastinal mass lesion

2003 ◽  
Vol 48 (2) ◽  
pp. 39-42 ◽  
Author(s):  
Y Revilla
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Ikchan Jeon ◽  
Joon Hyuk Choi

Abstract Background Erdheim-Chester disease (ECD) is a rare, idiopathic, systemic non-Langerhans cell histiocytosis involving long bone and visceral organs. Central nervous system (CNS) involvement is uncommon and most cases develop as a part of systemic disease. We present a rare case of variant ECD as an isolated intramedullary tumor. Case presentation A 75-year-old female patient with a medical history of diabetes and hypertension presented with sudden-onset flaccid paraparesis for 1 day. Neurological examination revealed grade 2–3 weakness in both legs, decreased deep tendon reflex, loss of anal tone, and numbness below T4. Leg weakness deteriorated to G1 before surgery. Preoperative magnetic resonance imaging (MRI) and 18F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) showed an intramedullary mass lesion at T2-T4 with no systemic lesion, which was heterogeneous enhancement pattern with cord swelling and edema from C7 to T6. Gross total removal was achieved for the white-gray-colored and soft-natured intramedullary mass lesion with an ill-defined boundary. Histological finding revealed benign histiocytic proliferation with foamy histiocytes and uniform nuclei. We concluded it as an isolated intramedullary ECD. The patient showed self-standing and walkable at 18-month with no evidence of recurrence and new lesion on spine MRI and whole-body FDG-PET/CT until sudden occurrence of unknown originated thoracic cord infarction. Conclusions We experienced an extremely rare case of isolated intramedullary ECD, which was controlled by surgical resection with no adjuvant therapy. Histological examination is the most important for final diagnosis, and careful serial follow-up after surgical resection is required to identify the recurrence and progression to systemic disease.


2011 ◽  
Vol 1 (2) ◽  
pp. 47-50
Author(s):  
Ghada M. Abbas ◽  
Athar A. Radwi

Azygos vein aneurysm and thrombosis are rare. It resembles a mediastinal mass that can be seen by chest radiograph, computed tomography, and magnetic resonance imaging. This case describes an elderly woman with a mediastinal mass due to azygos vein aneurysm and thrombosis. She was diagnosed by non-invasive procedures. The etiology of the azygos vein aneurysm was portal hypertension secondary to liver cirrhosis. Re-canalization was established by non-invasive management.


2002 ◽  
Vol 16 (6) ◽  
pp. 746-750 ◽  
Author(s):  
Mehmet Ö. Öksüz ◽  
Carsten Altehoefer ◽  
Jan T. Winterer ◽  
Marisa Windfuhr-Blum ◽  
Manuela Kleinschmidt ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Maxine Darke ◽  
Anil Dasyam ◽  
Matthew Then ◽  
Kavita Varma ◽  
Amir A. Borhani ◽  
...  

Hibernomas, especially located in the mediastinum, are extremely rare benign tumors, which are important to consider in the differential diagnosis of a heterogeneously enhancing mass with areas of fat attenuation on imaging of an often incidentally discovered mass. Other common possibilities in the differential include malignant tumors, such as liposarcoma, hence histopathology is usually required to confirm the diagnosis. Hibernomas often follow the distribution of sites of persistence of brown fat in adults, and intrathoracic locations are unusual. We present a very rare case of a mediastinal hibernoma in a 53-year-old woman. She presented to the emergency department with severe, progressive right neck and shoulder pain with radiation down her arm and was found to have a right apical posterior mediastinal mass on imaging. Initial radiographs of the shoulder showed a soft tissue mass within the apical right hemithorax. Further imaging with CT revealed a well circumscribed, heterogeneously enhancing mass with areas of fat attenuation. Pathology confirmed the diagnosis of mediastinal hibernoma, and the mass was completely excised. Fourteen months after surgery, the patient had a normal chest radiograph, and thirty-two months after surgery, she remains asymptomatic.


2006 ◽  
Vol 42 (8) ◽  
pp. 410-412 ◽  
Author(s):  
Núria Abad Santamaría ◽  
María José Gareía Díez ◽  
María José Pavón Fernández ◽  
A.M. Encabo Motiño ◽  
Susana Flórez Martín ◽  
...  
Keyword(s):  

2015 ◽  
Vol 76 (01) ◽  
pp. e140-e145 ◽  
Author(s):  
D. Jussen ◽  
C. Musahl ◽  
S. Scheil-Bertram ◽  
K. Wernecke ◽  
P. Horn ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document