scholarly journals Focal Xanthogranulomatous Pyelonephritis with Pulmonary Lesions on the Background of Type Two Diabetes Mellitus

2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Ahmad Enshaei ◽  
Arash A. Boora ◽  
Diana Taheri ◽  
Zahra Changizi ◽  
Nahid Bahmani
Keyword(s):  
Bacterial Infection ◽  
Renal Calculi ◽  
Large Mass ◽  
Xanthogranulomatous Pyelonephritis ◽  
Medical Attention ◽  
Pulmonary Lesions ◽  
Chronic Inflammatory Condition ◽  
The Right ◽  
Type Two Diabetes ◽  
Staghorn Renal Calculi

Focal Xanthogranulomatous pyelonephritis is a rare chronic inflammatory condition of kidneys which usually is associated with postrenal obstruction or renal stone leading to chronic bacterial infection and eventually chronic glomerular inflammation. About 90% of cases are of the diffuse type and associated with staghorn renal calculi. The case presented in this paper is of the focal type in a 58-year-old diabetic female. Interestingly she did not have symptoms or laboratory presentation of chronic renal bacterial infection except for elevated ESR. She sought medical attention due to severe pulmonary infection of the background of morbid obesity. Imaging studies revealed several pulmonary lesions and a large mass of the right kidney which was indistinguishable from renal malignancy. After surgical resection of the right kidney, the lesion is pathologically diagnosed to be a focal Xanthogranulomatous pyelonephritis. The pulmonary lesions were spontaneously resolved about three months following right nephrectomy.

scholarly journals Intrascrotal lipoblastoma in adulthood

2019 ◽  
Vol 12 (12) ◽  
pp. e231320
Author(s):  
Mário José Pereira-Lourenço ◽  
Duarte Vieira-Brito ◽  
João Pedro Peralta ◽  
Noémia Castelo-Branco
Keyword(s):  
Case Report ◽  
Magnetic Resonance ◽  
S100 Protein ◽  
Surgical Excision ◽  
Large Mass ◽  
Histological Diagnosis ◽  
Physical Exam ◽  
Nodular Lesion ◽  
Inferior Portion ◽  
The Right

This case report describes the case of a 37-year-old man that noticed an intrascrotal right mass with 1 month of evolution. During physical exam presented with a large mass at the inferior portion of the right testicle, clearly separated from the testicle, with a tender consistency and mobile. An ultrasound was performed that showed a solid and subcutaneous nodular lesion, extra testicular, heterogeneous, measuring 7.2 cm. Pelvic magnetic resonance imageMRI showed a lesion compatible with a lipoma. The patient was subjected to surgical excision of the lesion by scrotal access, having histology revealed a lipoblastoma (LB) of the scrotum. Histological diagnosis was obtained by microscopic characteristics (well-circumscribed fatty neoplasm) and immunohistochemistry (stains for CD34, S100 protein and PLAG1 were positive; stains for MDM2 and CDK4 were negative). LB is extremely rare after adolescence in any location, being this first described case of intrascrotal LB described in adulthood.

scholarly journals Resection of primary cardiac angiosarcoma infiltrating the right atrioventricular junction and tricuspid valve: a case report

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Lubna Bakr ◽  
Hussam AlKhalaf ◽  
Ahmad Takriti
Keyword(s):  
Surgical Resection ◽  
Tricuspid Valve ◽  
Right Atrium ◽  
Large Mass ◽  
Small Mass ◽  
Malignant Tumours ◽  
Atrioventricular Junction ◽  
Cardiac Angiosarcoma ◽  
Complete Surgical Resection ◽  
The Right

Abstract Background Primary cardiac tumours are extremely rare. Most of them are benign. Sarcomas account for 95% of the malignant tumours. Prognosis of primary cardiac angiosarcoma remains poor. Complete surgical resection is oftentimes hampered when there is extensive tumour involvement into important cardiac apparatus. We report a case of cardiac angiosarcoma of the right atrium and ventricle, infiltrating the right atrioventricular junction and tricuspid valve. Case presentation Initially, a 22-year-old man presented with dyspnoea. One year later, he had recurrent pericardial effusion. Afterwards, echocardiography revealed a large mass in the right atrium, expanding from the roof of the right atrium to the tricuspid valve. The mass was causing compression on the tricuspid valve, and another mass was seen in the right ventricle. Complete resection of the tumour was impossible. The mass was resected with the biggest possible margins. The right atrium was reconstructed using heterologous pericardium. The patient’s postoperative course was uneventful. Postoperative echocardiography showed a small mass remaining in the right side of the heart. Histopathology and immunohistochemistry confirmed the diagnosis of angiosarcoma. The patient underwent adjuvant chemotherapy and radiotherapy later on. He survived for 1 year and 5 days after the surgery. After a diagnosis of lung and brain metastases, he ended up on mechanical ventilation for 48 h and died. Conclusions Surgical resection combined with postoperative chemotherapy and radiotherapy is feasible even in patients with an advanced stage of cardiac angiosarcoma when it is impossible to perform complete surgical resection.

Strategic lithotripsy using the Doli S EMSE 220 F-XP for the management of staghorn renal calculi

2010 ◽  
Vol 43 (1) ◽  
pp. 61-65 ◽  
Author(s):  
Ioannis Heretis ◽  
Charalampos Mamoulakis ◽  
Vaios Papadimitriou ◽  
Frank Sofras
Keyword(s):  
Renal Calculi ◽  
Staghorn Renal Calculi

scholarly journals ETMR-07. ETANTR: A RARE TUMOR IN A RESOURCE-LIMITED SETTING

2020 ◽  
Vol 22 (Supplement_3) ◽  
pp. iii324-iii324
Author(s):  
Julieta Hoveyan ◽  
Manushak Avagyan ◽  
Anna Avagyan ◽  
Ruzanna Papyan ◽  
Samvel Iskanyan ◽  
...  
Keyword(s):  
Survival Rates ◽  
Tumor Resection ◽  
Large Mass ◽  
Intrathecal Methotrexate ◽  
High Dose ◽  
Ongoing Research ◽  
Resource Limited ◽  
The Right ◽  
Immunohistochemical Analyses ◽  
Limited Setting

Abstract INTRODUCTION Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a rare aggressive brain tumor with low survival rates. There are about 80 cases reported in literature since 2000 when it was first described. There is no standard treatment scheme for ETANTR yet. CASE REPORT: A 2 years old boy presented with a month-long of headache and inability to hold his head. CT scan and MRI revealed a large mass in the right frontal lobe with midline shift. Subtotal tumor resection was done. Histological and immunohistochemical analyses was consistent with ETANTR in one laboratory and PNET in another. The second opinion suggested by the Center of Pediatric Oncology, Hematology and Immunology in Moscow the diagnosis ETANTR was confirmed. Taking into account certain similarities with medulloblastoma was decided to provide treatment according to HIT-2014 protocol. Control MRI done after 2 cycles of Block SKK Carboplatin/Etoposide found tumor progression and for that reason patient underwent second surgical resection. Considering the age of the child radiation therapy was not expedient and the decision was to continue treatment with HIT 2014 intensified regimen, which includes Cisplatin, Vincristine, Etoposide, Cyclophosphamide and intravenous High dose Methotrexate with intrathecal Methotrexate. Aiming to evaluate the effectiveness of treatment we are planning to perform MRI after this 2nd cycle of intensified regimen. DISCUSSION There are difficulties in diagnosis of rare types of cancers in Armenia. Since there is no approved treatment for ETANTR, there is a need for ongoing research to improve its prognosis.

Case 6.11

2014 ◽  
pp. 304-305
Author(s):  
Christine U. Lee ◽  
James F. Glockner
Keyword(s):  
Adrenal Gland ◽  
Signal Intensity ◽  
Adrenal Mass ◽  
Large Mass ◽  
Female Infant ◽  
Hepatic Parenchyma ◽  
The Right ◽  
T2 Weighted Images

1-month-old female infant with a renal or adrenal mass Axial fat-suppressed FSE T2-weighted images (Figure 6.11.1) reveal a large mass originating from the right adrenal gland with heterogeneously increased signal intensity. Extensive small hyperintense metastases essentially replace the visualized hepatic parenchyma. Axial fat-suppressed FSE images from the 6-week follow-up examination (...

Case 1.30

2014 ◽  
pp. 60-61
Author(s):  
Christine U. Lee ◽  
James F. Glockner
Keyword(s):  
Large Mass ◽  
Hepatic Veins ◽  
Axial Diffusion ◽  
Hepatic Lobe ◽  
Diffusion Weighted ◽  
The Right ◽  
Delayed Phase

82-year-old man with vomiting, jaundice, and abnormal CT Coronal SSFSE (Figure 1.30.1), axial fat-suppressed T2-weighted FSE (Figure 1.30.2), and axial diffusion-weighted (b=100 s/mm2) (Figure 1.30.3) images demonstrate a large mass in the central right hepatic lobe surrounding, but not occluding, the right hepatic veins. Axial arterial, portal venous, equilibrium, and delayed phase postgadolinium 3D SPGR images (...

Visual Diagnosis: Large Mass with Ulceration over the Right Shoulder

2019 ◽  
Vol 40 (8) ◽  
pp. e28-e31
Author(s):  
Vanessa Amaral ◽  
Joyce Tong ◽  
Kam Ching Chow ◽  
Jorge Sales Marques
Keyword(s):  
Large Mass ◽  
The Right ◽  
Visual Diagnosis

scholarly journals Head and tail pancreatic duct stones mimicking duplex staghorn renal calculi: A rare case

2020 ◽  
Vol 77 ◽  
pp. 523-526
Author(s):  
Adeodatus Yuda Handaya ◽  
Nurbudiono ◽  
Aditya Rifqi Fauzi ◽  
Joshua Andrew ◽  
Ahmad Shafa Hanif ◽  
...  
Keyword(s):  
Pancreatic Duct ◽  
Rare Case ◽  
Renal Calculi ◽  
Pancreatic Duct Stones ◽  
Staghorn Renal Calculi

scholarly journals Case of primary hepatic leiomyosarcoma successfully treated with laparoscopic right hepatectomy

2020 ◽  
Vol 13 (2) ◽  
pp. e233567 ◽  
Author(s):  
Stephanie Vella ◽  
Kelvin Cortis ◽  
David Pisani ◽  
James Pocock ◽  
Luca Aldrighetti
Keyword(s):  
Physical Examination ◽  
Surgical Resection ◽  
Epigastric Pain ◽  
Large Mass ◽  
Disease Recurrence ◽  
Right Hepatectomy ◽  
Liver Lobe ◽  
Laparoscopic Right Hepatectomy ◽  
The Right

We describe the case of a 77-year-old woman, presenting with non-specific epigastric pain. Physical examination and subsequent imaging revealed the presence of a large mass in the right liver lobe. This was shown to be a leiomyosarcoma on biopsy histology. Further investigation confirmed this to be a primary hepatic leiomyosarcoma with no evidence of metastases. The patient underwent successful surgical resection. She is currently under imaging follow-up, with no evidence of disease recurrence.

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