Takayasu’s arteritis and secondary membranous nephropathy: an exceptional association

2021 ◽  
Vol 14 (3) ◽  
pp. e237945
Author(s):  
Daniel Enos ◽  
Gonzalo Labarca ◽  
Mariel Hernandez ◽  
Gonzalo P Mendez

The association between Takayasu’s arteritis and membranous nephropathy is uncommon. We present the case of a 46-year-old man with Takayasu’s arteritis treated over 10 years by a multidisciplinary medical team. He had an atrophic left kidney due to arterial stenosis, with a basal creatinine of 1.59 mg/dL (140.55 µmol/l). Three years ago, he presented with full nephrotic syndrome, uncontrolled blood pressure, creatinine increases to 4.5 mg/dL (basal: 1.59 mg/dL), severe hypoalbuminaemia (1.4 g/dL) and albuminuria of 24.6 g per day. He underwent percutaneous biopsy of the right kidney that showed membranous nephropathy with negative PLA2R1 and positive IgG 1, 3 and 4 subclasses. After therapy with oral prednisone and cyclophosphamide, the patient’s kidney function improved, without recurrence of disease after 3 years of follow-up. Here, we present this extremely uncommon association of Takayasu’s arteritis and membranous nephropathy.

2017 ◽  
Vol 42 ◽  
pp. 93-100 ◽  
Author(s):  
Aytaç Gülcü ◽  
Naciye Sinem Gezer ◽  
Servet Akar ◽  
Nurullah Akkoç ◽  
Fatoş Önen ◽  
...  

2001 ◽  
Vol 31 (2) ◽  
pp. 246 ◽  
Author(s):  
Kyung Tae Kang ◽  
Myung Ho Jeong ◽  
Woo Kon Jeong ◽  
Sang Hyun Lee ◽  
Jay Young Rhew ◽  
...  

Stroke ◽  
1996 ◽  
Vol 27 (12) ◽  
pp. 2178-2182 ◽  
Author(s):  
Yu Sun ◽  
Ping-Keung Yip ◽  
Jiann-Shing Jeng ◽  
Bao-Show Hwang ◽  
Win-Hwan Lin

2012 ◽  
Vol 56 (2) ◽  
pp. 504-507 ◽  
Author(s):  
Domenico Angiletta ◽  
Davide Marinazzo ◽  
Gloria Guido ◽  
Martinella Fullone ◽  
Raffaele Pulli ◽  
...  

2009 ◽  
Vol 33 (2) ◽  
pp. 80-87
Author(s):  
Karen Broadbent ◽  
Zsolt Garami ◽  
Eric K. Peden ◽  
Alan Lumsden

2008 ◽  
Vol 51 (3) ◽  
pp. 196-200 ◽  
Author(s):  
Yusuke Fukuda ◽  
Kazuyuki Shirai ◽  
Yosuke Takamiya ◽  
Miller Nathan ◽  
Takahiro Mito ◽  
...  

2006 ◽  
Vol 23 (5) ◽  
pp. 353-360 ◽  
Author(s):  
Maria Elena Soto ◽  
Nilda Espinola-Zavaleta ◽  
Oscar Ramirez-Quito ◽  
Pedro A. Reyes

2010 ◽  
Vol 5 (6) ◽  
pp. 586-590 ◽  
Author(s):  
Balaji Srinivas ◽  
Vivek Joseph ◽  
Geeta Chacko ◽  
Vedantam Rajshekhar

Spinal extradural cysts do not normally present as a visible paraspinal mass or cause compression of the abdominal organs. The authors describe the case of a 9-month-old boy with multiple spinal extradural cysts. The largest of these cysts was along the right L-2 nerve root with significant extraspinal extension resulting in a visible slow-growing swelling in the right paraspinal region and radiological evidence of compression of the right kidney with hydronephrosis. Another large cyst along the left T-12 root caused radiologically evident compression of the left kidney but to a lesser degree. The patient also had monoparesis of the left lower limb and phenotypic features of Noonan syndrome. The authors performed marsupialization of the cysts, as well as repair of the fistula between the subarachnoid space and the cyst on the right side along the L-2 root and on the left side along the T-12 root. At 1-year follow-up, there was no paraspinal mass and the lower limbs exhibited normal power. Magnetic resonance imaging confirmed marked reduction in the size of the cysts and relief of the renal compression. To the authors' knowledge, their patient is the youngest reported in literature to have a spinal extradural cyst and also the first with the cyst presenting as a paraspinal mass.


2011 ◽  
Vol 11 (2) ◽  
pp. 132-136 ◽  
Author(s):  
Yael Eshet ◽  
Rachel Pauzner ◽  
Orly Goitein ◽  
Pnina Langevitz ◽  
Iris Eshed ◽  
...  

2019 ◽  
pp. 1-3
Author(s):  
Aïcha Ben Miled ◽  
Chadli Dziri ◽  
Hichem Jerraya ◽  
Ibtissem Bouasker ◽  
Mohamed Ali ◽  
...  

Adrenocortical carcinoma is a rare malignant tumor which can reach large sizes if it is nonfunctioning. In that situation, it can pose diagnosis dilemmas regarding the origin and the nature of the tumor. We reported a case of non-secreting and large right Adrenocortical carcinoma which arose in the posterior costophrenic angle mimicking a liver tumor. A 45-year-old man presented with a voluminous abdominal mass in the right upper quadrant. The different imaging modalities including ultrasound computed tomography and magnetic resonance imaging were discordant as regards the hepatic or the adrenal origin of the tumor. Percutaneous biopsy allowed to determine the diagnosis of the cortico-adrenal tumor. The patient underwent laparotomy. The tumor which arose from the right adrenal gland was resected. Pathology confirmed the diagnosis of adrenocortical carcinoma with histological factors of poor prognosis. The patient was given Mitotane as adjuvant therapy. After six years of follow-up, a tumor recurrence has been diagnosed.


Sign in / Sign up

Export Citation Format

Share Document