Case 7.8

Author(s):  
Christine U. Lee ◽  
James F. Glockner

85-year-old man with acute on chronic renal failure Coronal SSFSE (Figure 7.8.1), axial FSE (Figure 7.8.2), and axial diffusion-weighted (b=100 s/mm2) (Figure 7.8.3) images reveal a small left kidney with hydronephrosis of upper pole calyces. Nodular thickening involves the renal capsule and Gerota fascia, with larger nodules adjacent to the renal hilum and within the perinephric fat. Note also the right-sided renal cysts....

2017 ◽  
Vol 45 (1) ◽  
pp. 7
Author(s):  
Carolina Da Fonseca Sapin ◽  
Luísa Cerqueira Silva-Mariano ◽  
Andressa Dutra Piovesan ◽  
Cristina Gevehr Fernandes ◽  
Josaine Cristina da Silva Rappeti ◽  
...  

Background: Dioctophymiasis is a disease caused by the nematode Dioctophyme renale and is a relatively common condition in dogs. The parasite affects the kidney, especially the right, enters the kidney capsule and causes destruction and atrophy of the parenchyma. The lesion severity depends on the amount of parasites affecting the kidney, the duration of the infection, number of kidneys involved and concurrent occurrence of kidney disease. The disease’s clinical presentation may be asymptomatic or with nonspecific clinical signs. The diagnosis is based on ultrasound examination and the detection of eggs in urine, however, diagnosis is often reached only through necropsy or histopathology. This study aimed to analyze the dog kidney anatomical and pathological changes when parasitized by Dioctophyme renale.Materials, Methods & Results: The kidneys of 21 dogs diagnosed with dioctophymiasis were nephrectomized, analyzed by ultrasound and forwarded to macro and microscopic analysis. Macroscopically, the kidney size was measured as well as its renal capsule thicknes. The presences of dilatation of the renal pelvis and ureter, as well as changes of the capsule, were also observed. These fragments were collected and submitted for routine analysis and stained with hematoxylin and eosin. Histopathological examination was performed blindly by three evaluators. The intensity of fibrosis was evaluated by the presence or absence of infiltration, the absence or presence of parasite eggs and when present whether there was inflammatory tissue response, among other changes. All received organs were right kidneys and showed clear atrophy or absence of the parenchyma. The kidney size ranged from 3,8x2,5x1,3 cm to 8,4x8,2x4,0 cm and the capsule thickness between 0.1 and 3.6cm. In renal capsule were observed whitish, irregular and firm plates (10 out of 21 cases) and papilliform projections (4 out of 21). In two specimens were identified cases of hydroureter and hydronephrosis. Microscopically, all specimens had some degree of fibrosis which replaced the renal parenchyma, six classified as mild, ten were moderate and five intense. In 13 cases there was intense deposition of parasite eggs and 18 cases showed inflammatory infiltrate of which one was pyogranulomatous and one granulomatous. Papilliform projections were observed in six out of 21 cases (composed of connective tissue proliferation and neovascularization), there was also hyperplasia of the pelvis transition epithelial (6 out of 21) and osseous metaplasia of the renal capsule (4 out of 21). The vessels walls were hypertrophic in nine out of 21 cases.Discussion: The diagnosis of dioctophymiasis was performed by ultrasonography. All 21 kidneys analyzed were rights; this is related to the parasite penetration in the duodenal wall, which tends to migrate by anatomic proximity to the right kidneys. Dioctophyme renale feeds through digestion and ingestion of the renal parenchyma by the action of parasite’s oesophageal enzymes causing progressive destruction of the cortical and medullar layers and consequently the proliferation of fibrous tissue. In this study, different intensities of fibrosis were observed. Bone metaplasia characterizes the chronicity of the process and the connective tissue’s attempt to adapt. Animals affected by dioctophymiasis often develop chronic renal failure. Chronic renal failure is characterized by continuous and irreversible morphologic changes in the renal parenchyma with loss of nephron components and the formation of a vicious cycle of replacement by fibrous connective tissue. The hypertrophy of vascular epithelium observed in six cases of this study may be associated with fibrous connective tissue proliferation stimulus. The injuries described here may be related to the parasitosis late diagnosis.


Nephron ◽  
1982 ◽  
Vol 30 (1) ◽  
pp. 85-88 ◽  
Author(s):  
Robert D. Okada ◽  
Michael A. Platt ◽  
Jay Fleishman

Author(s):  
Christine U. Lee ◽  
James F. Glockner

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 (...


2000 ◽  
Vol 3 (5) ◽  
pp. 472-478 ◽  
Author(s):  
Keshani de Silva ◽  
Vivienne Tobias ◽  
Gad Kainer ◽  
Bruce Beckwith

We report a case of a 9-year-old boy with focal, segmental glomerulosclerosis who, following peritoneal dialysis, underwent renal transplantation and bilateral nephrectomy. The kidneys showed histological features of embryonal hyperplasia of Bowman's capsular epithelium, an uncommon lesion that is seen most often in patients with chronic renal failure who are being maintained on dialysis. In addition, a 1-cm tumor in the left kidney showed features of metanephric adenoma. Although both lesions are uncommon, they share many similarities on a morphological, immunohistochemical, and ultrastructural basis. This association has not been previously reported and may shed some light on the histogenesis of these recently described lesions.


2021 ◽  
Vol 22 (2) ◽  
pp. 155-156
Author(s):  
Mohammed Mehedi Al Zahid Bhuiyan ◽  
Azmal Kabir Sarker ◽  
Hongyoon Choi ◽  
Minseok Suh ◽  
Gi Jeong Cheon

A 57-year-old female patient underwent left breast-conserving surgery with sentinel lymph node biopsy for Left breast carcinoma (stage IIA). The patient had hypertension and diabetes mellitus. Other findings include multiple hepatic cyst, bilateral renal cysts and uterine myoma. She had no significant renal symptoms and her liver &renal function test were normal.She was sent for Technetium-99m-methylene diphosphonate (99mTc-MDP) bone scan. There was a large area of intense tracer concentration in the region of right sacro-iliac (SI) joint which appeared like an osteoblastic metastasis at first glance. However, absence of uptake in the right renal fossa with the left kidney being normal in position contemplated the probability of right-sidedpelvickidneywhich was confirmed later by a contrast enhanced computerized tomography (CT) scan of abdomen that showed a pelvic right kidney overlying the sacrum. Bangladesh J. Nuclear Med. 22(2): 155-156, Jul 2019


2018 ◽  
Vol 12 (1) ◽  
Author(s):  
Luigi Pais dei Mori

[Nursing responsibility profiles in a case of forearm amputation by wrong infusion practice in a premature newborn]This article refers to the case of a premature newborn twin (23 weeks of gestation + 6). Of the two brothers, only one survived, in a highly compromised state of health that led to a notable and dramatic series of clinical events: infectious complications, chronic renal failure, viscera herniation, intestinal perforation, and thrombocytopenia, treated with various infusions of platelet concentrates.During an infusion of platelet concentrate, an extravasation occurred with important tissue infarction. The lesion created, secondary to ischemic necrosis, evolves into dry necrosis, from the hand to the whole forearm, and leads to the amputation of the right forearm, despite the various attempts, pharmacological and surgical, experienced to avoid the extrema ratio.The purpose of this article is to analyze what happened considering scientific clinical evidence and the profile of responsibilities related to nursing practice.


2008 ◽  
Vol 74 (8) ◽  
pp. 1094-1099 ◽  
Author(s):  
Christie P. Thomas ◽  
Jerold C. Erlandson ◽  
Emma L. Edghill ◽  
Andrew T. Hattersley ◽  
Alan H. Stolpen

Author(s):  
Christine U. Lee ◽  
James F. Glockner

62-year-old woman with ADPKD and new onset anorexia, weight loss, night sweats, and fever Coronal SSFP (Figure 7.6.1) and axial fat-suppressed SSFP (Figure 7.6.2) images reveal enlarged, polycystic kidneys. There is a relatively hypointense mass in the lower pole of the left kidney. Axial diffusion-weighted image (b=800 s/mm...


Author(s):  
Christine U. Lee ◽  
James F. Glockner

50-year-old woman being evaluated for common variable immunodeficiency Coronal SSFSE (Figure 2.37.1), axial fat-suppressed T2-weighted FSE (Figure 2.37.2), and axial diffusion-weighted (b=100 s/mm2) (Figure 2.37.3) images demonstrate a heterogeneous mass with lobulated margins in the right hepatic lobe, as well as extensive adenopathy in the celiac axis, porta hepatis, and portocaval space. Note also moderate splenomegaly. Arterial, portal venous, equilibrium, and delayed phase postgadolinium 3D SPGR images (...


2015 ◽  
Vol 76 (1) ◽  
Author(s):  
Cinzia Perrino ◽  
Laura Scudiero ◽  
Maria Piera Petretta ◽  
Gabriele Giacomo Schiattarella ◽  
Mario De Laurentis ◽  
...  

Total occlusion of the abdominal aorta is unusual, and potentially catastrophic. It occurs in patients with advanced atherosclerotic occlusive disease, and can cause severe ischemic manifestations, depending on the site of obstruction. Prompt and appropriate diagnostic and therapeutic approaches are important whenever this condition is suspected, in order to avoid a fatal outcome. The development of a complex network of collaterals may prevent the manifestation of acute ischemic phenomena, and cause a delay in diagnosis and treatment. Here we report the clinical case of a 59-year-old man who was referred to our Department for evaluation of renal failure and refractory hypertension. Ultrasonography and 99mTc-DTPA scintigraphy showed a shrunken, non-functioning left kidney, while CT angiography and aortography showed the complete occlusion of the aorta from below the right renal artery down to the bifurcation of both common iliac arteries, with a critical stenosis of the origin of the right renal artery, an occlusion of the left renal artery as well as of the origin of the inferior mesenteric artery. The patient was referred to the surgery department for aorto-bifemoral bypass surgery and re-implantation of the right renal artery.


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