Lymphocytic vasculitis a paraneoplastic syndrome associated with Renal Cell Carcinoma

2016 ◽  
Vol 4 (2) ◽  
pp. 41
Author(s):  
H Basavanagowdappa ◽  
Prathibha Pereira ◽  
KC Shashidhar ◽  
Chaithra ◽  
Ranganath ◽  
...  
2019 ◽  
Vol 114 (1) ◽  
pp. S1422-S1423
Author(s):  
Barrett Attarha ◽  
Satish Maharaj ◽  
Ciel Harris ◽  
Ron Schey ◽  
Ammar Nassri ◽  
...  

2012 ◽  
Vol 21 (4) ◽  
pp. 370-374 ◽  
Author(s):  
Guan-Xiong Ding ◽  
Ning-Hong Song ◽  
Chen-Chen Feng ◽  
Guo-Wei Xia ◽  
Hao-Wen Jiang ◽  
...  

2017 ◽  
Vol 13 ◽  
pp. 101-103
Author(s):  
John M. DiBianco ◽  
Julie Y. An ◽  
Sally Tanakchi ◽  
Zachary Stanik ◽  
Aidan McGowan ◽  
...  

2006 ◽  
Vol 120 (3) ◽  
pp. 237-239 ◽  
Author(s):  
K Saravanan ◽  
S T Baer ◽  
A Meredith ◽  
A Dyson ◽  
Jan von der Werth

Benign mucous membrane pemphigoid is a rare autoimmune disorder affecting the upper aero-digestive tract and conjunctivae. This is a case presentation of benign mucous membrane pemphigoid affecting the oral mucosa, pharynx, oesophagus and larynx, leading to cicatricial lesions in the pharynx and larynx, causing dysphagia, hoarseness and stridor. The alternative forms of management for laryngeal scarring due to this disease are explained. The patient was later diagnosed with advanced renal cell carcinoma, raising the possibility of cicatricial pemphigoid manifesting as a paraneoplastic syndrome of underlying renal cell carcinoma.


2018 ◽  
Vol 39 (4) ◽  
pp. 546
Author(s):  
Mayank Jain ◽  
Joy Varghese ◽  
KM Muruganandham ◽  
Jayanthi Venkataraman

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Dominik Dabrowski ◽  
Ekin Ozluk ◽  
Silvia Barbeito ◽  
Eric X. Wei

Renal cell carcinoma (RCC) is the predominant renal malignancy in adults. Of the four general subtypes, papillary renal cell carcinoma (P-RCC) is the second most common and can be subdivided into type I, type II, and a mixture of type I and II. Focal segmental glomerulosclerosis (FSGS) is the most common glomerulopathy at all ages, and it can be seen as a paraneoplastic syndrome. RCC, in general, is known to present with many paraneoplastic syndromes, and glomerulopathies are among these. Rarely, RCC and glomerulopathies may overlap in the same patient. Here, we report a 58-year-old male with a past medical history of FSGS and chronic kidney disease (CKD), stage III, who was found to have an incidental renal mass that was later diagnosed as type II P-RCC. The histology showed pseudostratified tumor cells with an eosinophilic cytoplasm that formed papillary configurations and displayed areas of necrosis. The prior FSGS diagnosis exhibited segmental sclerosis, refractory tufts, and capillary membrane wrinkling. A period of 1.5 years elapsed between the diagnosis of the glomerulopathy and the malignancy. The tumor was found to be at stage TIb. To our knowledge, this may be the first reported case of usual-type FSGS as paraneoplastic glomerulopathy (PG) preceding P-RCC. Because FSGS only sparingly affects the kidney and is a common glomerulopathy in adults, it is reasonable to complete comprehensive diagnostic studies and commence medically necessary treatment, especially in the background of other renal comorbidities. These preexisting comorbidities may be associated with malignancy very early in its course. The probability of RCC-associated paraneoplastic glomerulopathy is low, which means an already incidentally found renal mass may conceal a serpentine paraneoplastic syndrome. A more developed understanding of these manifestations can lead experienced clinicians to suspect and possibly uncover an insidious RCC before it advances.


1985 ◽  
Vol 78 (4) ◽  
pp. 682-686 ◽  
Author(s):  
Nancy A. Dawson ◽  
Charles F. Barr ◽  
Barbara M. Alving

2014 ◽  
Vol 70 (1) ◽  
pp. 61-64 ◽  
Author(s):  
E. Naert ◽  
J. L. De Bleecker ◽  
N. Lumen ◽  
S. Rottey

2008 ◽  
Vol 90 (3) ◽  
pp. 279-281 ◽  
Author(s):  
Vijay Johnson ◽  
Norman Friedman ◽  
Nairmeen Awad Haller ◽  
Christian Hagel

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