scholarly journals Spleno-adrenal fusion mimicking an adrenal metastasis of a renal cell carcinoma: A case report and embryological background

Open Medicine ◽  
2020 ◽  
Vol 16 (1) ◽  
pp. 087-094
Author(s):  
Zbyněk Tüdös ◽  
Paulína Szász ◽  
Lucia Veverková ◽  
František Hruška ◽  
Igor Hartmann ◽  
...  

AbstractFoci of splenic tissue separated from the spleen can occur as a congenital anomaly. Isolated nodules of splenic tissue are called accessory spleens or spleniculli. However, nodules of splenic tissue can merge with other organs during embryonic development, in which case we speak of spleno-visceral fusions: most often, they merge with the tail of the pancreas (thus forming spleno-pancreatic fusion or an intrapancreatic accessory spleen), with the reproductive gland (i.e., spleno-gonadal fusion), or with the kidney (i.e., spleno-renal fusion). Our case report describes the fusion of heterotopic splenic tissue with the right adrenal gland, which was misinterpreted as a metastasis of a renal cell carcinoma. To the best of our knowledge, this is the first reported case of spleno-adrenal fusion. Spleno-visceral fusions usually represent asymptomatic conditions; their main clinical significance lies in the confusion they cause and its misinterpretation as tumors of other organs. We believe that the cause of retroperitoneal spleno-visceral fusions is the anomalous migration of splenic cells along the dorsal mesentery to the urogenital ridge, together with primitive germ cells, at the end of the fifth week and during the sixth week of embryonic age. This theory explains the possible origin of spleno-visceral fusions, their different frequency of occurrence, and the predominance of findings on the left side.

CASE ◽  
2020 ◽  
Vol 4 (4) ◽  
pp. 274-277
Author(s):  
Ahmed Abdelfattah ◽  
Mohamed El Wazir ◽  
Yehia Z. Ali ◽  
Jwan Naser ◽  
Brandon M. Wiley

2008 ◽  
Vol 32 (1) ◽  
pp. 159-160 ◽  
Author(s):  
JUNG-HO LEE ◽  
PAIK-KWON LEE ◽  
SANG-TAE AHN ◽  
DEUK-YOUNG OH ◽  
JONG-WON RHIE ◽  
...  

F1000Research ◽  
2013 ◽  
Vol 2 ◽  
pp. 263 ◽  
Author(s):  
Arvind Ganpule ◽  
Jitendra Jagtap ◽  
Sanika Ganpule ◽  
Amit Bhattu ◽  
Shailesh Soni ◽  
...  

We present a case of Xanthogranulomatous pyelonephritis mimicking as a renal cell carcinoma. This was an elderly lady who presented with pyonephrosis due to urolithiasis. On evaluation she was found to have a space occupying mass in the right kidney. Further investigations revealed an enhancing tumor with renal vein thrombus and paracaval lymphadenopathy. Subsequent histopathology showed evidence of XGPN with no malignancy. This case report highlights the fact there are a number of imaging and clinical overlaps in the diagnosis, assessment and management of this entity.


2010 ◽  
Vol 140 ◽  
pp. S76-S77
Author(s):  
Ugur Canpolat ◽  
Banu Evranos ◽  
Sercan Okutucu ◽  
Hikmet Yorgun ◽  
Ergun Baris Kaya ◽  
...  

2006 ◽  
Vol 92 (6) ◽  
pp. 549-551 ◽  
Author(s):  
Antonio Manzelli ◽  
Piero Rossi ◽  
Adriano De Majo ◽  
Giorgio Coscarella ◽  
Iwona Gacek ◽  
...  

In this paper, we describe a case of a 73-year old female with late skeletal muscle metastases from a clear-type renal cell carcinoma 8 years after total nephrectomy. The metastases were located in the right femoral quadriceps, in the sartorius muscle and adductor magnus muscle. A full clinical work-up was performed with blood examinations, radiological and pathological assessment. A complete surgical resection with a wide margin was performed for all lesions, and the final pathological report deposed for metastatic renal carcinoma clear-type cells. In this case report, we discuss the crucial rule of accurate radiological and pathological assessment and aggressive surgical management.


2020 ◽  
Vol 34 ◽  
pp. 205873842093161
Author(s):  
Xi Xie ◽  
Ning Wang ◽  
Jingjing Xiang ◽  
Huadong He ◽  
Xuliang Wang ◽  
...  

We presented the clinical data of one patient with renal cell carcinoma associated with idiopathic thrombocytopenic purpura in this case report. We reported a 56-year-old man who presented with petechiae and ecchymoses. Laboratory studies showed the platelet count of 2 × 109/L and an abdominal computed tomography (CT) scan revealed tumors in the right renal. There were purpura on the legs and cough without abdominal pain and melena at this time. Idiopathic thrombocytopenic purpura was diagnosed according to the clinical symptoms and laboratory test. The patient received radical nephrectomy for renal carcinoma, and his idiopathic thrombocytopenic purpura was cured after the surgery. Pathological biopsy confirmed it was renal clear cell carcinoma. The patient has been followed up for more than 3 months after surgery, and the ecchymoses had not been recurred and the patient’s thrombocytopenia was recovered. Idiopathic thrombocytopenic purpura associated with kidney cancer is rare. The patient in this case report was treated with radical nephrectomy, and the effectiveness of idiopathic thrombocytopenic purpura was satisfactory.


Author(s):  
Dragoslav Basic ◽  
Ljubinka Jankovic-Velickovic ◽  
Ivan Ignjatovic ◽  
Jovan Hadzi-Djokic ◽  
Andrej Veljkovic

Introduction. Simultaneous ipsilateral coexistence of renal cell carcinoma (RCC) and upper urinary tract urothelial carcinoma (UTUC) rarely occurs. Balkan endemic nephropathy (BEN) is a chronic degenerative tubulointerstitial renal disease, strongly associated with UTUC. Case outline. ? 60-year-old man from the region of BEN was referred to our clinic due to right flank pain, fever, and purulent discharge from the cutaneous fistulous opening in the right lumbar area. Multislice computed tomography urography scan showed right-side pyonephrosis and nephrocutaneous fistulous tract between the kidney and the skin in the right lumbar region. Cystoscopy detected papillary tumor protruding from the right ureteric orifice. Right-side nephroureterectomy with bladder cuff excision (BCE) was performed. Histopathological examination revealed rhabdoid RCC of the kidney and multifocal urothelial carcinoma of the ureter. Conclusion. Our case report and literature review indicate that due to rising incidence of multiple primary malignant neoplasms, when treating patients with RCC or UTUC, and especially those from the region of BEN, one should keep in mind the likelihood of synchronous or metachronous occurrence of these tumors.


2019 ◽  
Vol 47 (6) ◽  
pp. 2728-2739
Author(s):  
Xu Cheng ◽  
Zhichao Huang ◽  
Daiqiang Li ◽  
Yinhuai Wang

Introduction Primary renal lymphoma is a rare malignant lymphoma that is difficult to differentiate from renal cell carcinoma. Positron emission tomography/computed tomography and image-guided percutaneous biopsy are valuable tools for diagnosis. Case report A 64-year-old woman presented with a 2-year history of repeated right waist pain and a 1-month history of nausea, vomiting, and frequent and urgent urination. A computed tomography scan showed a huge mass that was initially considered to be renal cell carcinoma at the upper pole of the right kidney. The mass had invaded the renal pelvis, narrowed the right renal artery, and constricted the inferior vena cava and liver. Postoperative examination of the tumor confirmed lymphoma. We herein present this case and its multidisciplinary team management. Conclusion Multidisciplinary team management is efficient for preoperative assessment and surgery in difficult and high-risk cases. Based on our literature review, we suggest biopsy before chemotherapy whenever possible. Chemotherapy can be implemented after surgery for better survival outcomes.


2021 ◽  
Vol 35 ◽  
pp. 101551
Author(s):  
Cyro Rezende Laghi ◽  
Bruno Costa do Prado ◽  
Germano de Freitas Dan ◽  
Gustavo Ruschi Bechara ◽  
Bruna Afonso Venturini ◽  
...  

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