keyword
https://read.qxmd.com/read/38490885/robotic-assisted-pediatric-thoracic-and-abdominal-tumor-resection-an-initial-multi-center-review
#21
JOURNAL ARTICLE
Wendy Jo Svetanoff, Michela Carter, Karen A Diefenbach, Marc Michalsky, Daniel DaJusta, Edward Gong, Timothy B Lautz, Jennifer H Aldrink
INTRODUCTION: Robotic-assisted minimally invasive surgery (RA-MIS) for tumor resection is an emerging technology in the pediatric population with significant promise but unproven safety and feasibility. METHODS: A multi-center retrospective review of patients ≤18 years undergoing RA-MIS tumor resection from December 2015-March 2023 was performed. Patient demographics, perioperative variables, and complication rates were analyzed. RESULTS: Thirty-nine procedures were performed on 38 patients (17 thoracic, 22 abdominal); 37% female and 68% non-Hispanic White...
February 26, 2024: Journal of Pediatric Surgery
https://read.qxmd.com/read/38483608/nutritional-status-as-a-predictive-factor-for-paediatric-tuberous-sclerosis-complex-associated-kidney-angiomyolipomas-a-retrospective-analysis
#22
JOURNAL ARTICLE
Andrew Limavady, Matko Marlais
UNLABELLED: The purpose of this study is to determine the predictive factors of tuberous sclerosis complex (TSC)-associated kidney disease and its progression in children. Retrospective review of children with TSC in a tertiary children's hospital was performed. Relevant data were extracted, and Cox proportional hazards regression was used to establish predictors of kidney lesions. Logistic regression was conducted to identify factors predicting chronic kidney disease (CKD) and high-risk angiomyolipomas (above 3 cm)...
March 14, 2024: European Journal of Pediatrics
https://read.qxmd.com/read/38479126/hepatic-angiomyolipoma-masquerading-as-abdominal-pain-a-case-report
#23
Laxman Khadka, Prajjwol Luitel, Sujan Paudel, Nischal Neupane, Laligen Awale, Abhishek Bhattarai
INTRODUCTION AND IMPORTANCE: Hepatic angiomyolipoma (HAML) is a rare liver tumor composed of blood vessels, smooth muscle, and fat cells. HAML occurs across a wide age range, with symptoms including abdominal discomfort, bloating, and weight loss. Diagnosis is challenging due to varied imaging appearances, but histopathological examination supplemented by immunohistochemical analysis, particularly using HMB-45, is definitive. CASE PRESENTATION: A 33-year-old man presented with a two-year history of right upper quadrant abdominal pain, occasionally relieved with analgesics but worsening over the past month and a half...
March 11, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38464581/multiple-renal-angiomyolipomas-with-asymptomatic-nontraumatic-pulmonary-fat-embolus-a-case-report
#24
Hourieh Soleimani, Masoud Pezeshki Rad, Donya Farrokh, Ehsan Hassannejad, Asma Payandeh, Sepideh Zahedi, Neda Karimabadi
Although retroperitoneal bleeding and massive hematuria are potential complications of angiomyolipoma (AML), the pulmonary embolism as a presenting symptom is extremely rare. It is important to be aware that benign AMLs can present with pulmonary fat embolism.
March 2024: Clinical Case Reports
https://read.qxmd.com/read/38459571/patients-and-physicians-awareness-of-clinical-symptoms-and-disease-severity-in-tuberous-sclerosis-complex
#25
JOURNAL ARTICLE
Matthias Sauter, Lea Weber, Dominik Jung, Michael Weremko, Dorothea Bachmann, Michael Fischereder, Hagen Sjard Bachmann
Tuberous sclerosis complex (TSC) is a rare inherited disease with the potential to affect virtually every organ system. Clinical presentation is age- and partly sex-dependent and varies broadly with respect to disease manifestations including treatment-refractory epilepsy, intellectual disability and TSC-associated neuropsychiatric disorders, chronic kidney disease or progressive lung function decline. Given the complexity of this disease, multidisciplinary care in specialized TSC centres is recommended. We aimed to elucidate the state of knowledge of patients/caregivers and physicians on individual disease manifestations...
March 8, 2024: Orphanet Journal of Rare Diseases
https://read.qxmd.com/read/38444661/clinical-tomographic-and-functional-comparison-of-sporadic-and-tuberous-sclerosis-complex-associated-forms-of-lymphangioleiomyomatosis-a-retrospective-cohort-study
#26
JOURNAL ARTICLE
Martina Rodrigues Oliveira, Mark Wanderley, Carolina Salim Gonçalves Freitas, Ronaldo Adib Kairalla, Rodrigo Caruso Chate, Alexandre Franco Amaral, Fabio Eiji Arimura, Luciana Paula Samorano, Elieser Hitoshi Watanabe, Carlos Roberto Ribeiro Carvalho, Bruno Guedes Baldi
BACKGROUND: Lymphangioleiomyomatosis (LAM) is a rare disease that can occur sporadically (S-LAM) or associated with the tuberous sclerosis complex (TSC-LAM). The natural history of LAM is not completely understood, including whether there is a difference between the clinical courses of the two forms. This study aimed to compare the clinical, functional and tomographic features between S-LAM and TSC-LAM, and evaluate the annual rates of change in lung function. METHODS: This retrospective cohort study included patients with LAM followed up between 1994 and 2019...
March 2024: ERJ Open Research
https://read.qxmd.com/read/38440714/usefulness-of-fluorescent-ureteral-catheter-during-laparoscopic-residual-ureterectomy
#27
Tomoko Honda, Yuki Matsuoka, Yu Osaki, Yoichiro Tohi, Hirohito Naito, Takuma Kato, Homare Okazoe, Rikiya Taoka, Nobufumi Ueda, Mikio Sugimoto
INTRODUCTION: There have been reports of surgery for residual ureteral tumors, most of them involved open surgeries. Herein, we report a case of retroperitoneal scopic left ureteral resection and partial cystectomy, performed by placing a fluorescent ureteral catheter in the residual ureter. CASE PRESENTATION: A 79-year-old man was admitted to our hospital with a chief complaint of gross hematuria. He had undergone transperitoneal left radical nephrectomy due to angiomyolipoma 20 years ago...
March 2024: IJU case reports
https://read.qxmd.com/read/38413459/uri-cads-a-fully-automated-computer-aided-diagnosis-system-for-ultrasound-renal-imaging
#28
JOURNAL ARTICLE
Miguel Molina-Moreno, Iván González-Díaz, Maite Rivera Gorrín, Víctor Burguera Vion, Fernando Díaz-de-María
Ultrasound is a widespread imaging modality, with special application in medical fields such as nephrology. However, automated approaches for ultrasound renal interpretation still pose some challenges: (1) the need for manual supervision by experts at various stages of the system, which prevents its adoption in primary healthcare, and (2) their limited considered taxonomy (e.g., reduced number of pathologies), which makes them unsuitable for training practitioners and providing support to experts. This paper proposes a fully automated computer-aided diagnosis system for ultrasound renal imaging addressing both of these challenges...
February 27, 2024: J Imaging Inform Med
https://read.qxmd.com/read/38410750/case-report-if-it-is-not-asthma-think-of-lymphangioleiomyomatosis-in-younger-female-patients
#29
Malene Helligsø Kirkeby, Elisabeth Bendstrup, Hanne Krogh Rose
Lymphangioleiomyomatosis (LAM) is a rare lung disease predominantly affecting women, and it is characterized by the proliferation of smooth muscle cells and cystic lung destruction. LAM diagnosis is challenging due to varied clinical presentations and resemblance to common conditions such as asthma. We present two female cases where LAM was initially misdiagnosed. Case 1 describes a woman treated for asthma-chronic obstruction pulmonary disease overlap syndrome, while also undergoing treatment with vascular endothelial growth factor (VEGF) inhibitor pazopanib for a retroperitoneal leiomyoma, the latter responding well to treatment...
2024: Frontiers in Medicine
https://read.qxmd.com/read/38398226/safety-and-diagnostic-efficacy-of-image-guided-biopsy-of-small-renal-masses
#30
JOURNAL ARTICLE
Muhamad Serhal, Sean Rangwani, Stephen M Seedial, Bartley Thornburg, Ahsun Riaz, Albert A Nemcek, Kent T Sato, Kent T Perry, Bonnie Choy, Robert J Lewandowski, Andrew C Gordon
INTRODUCTION: Image-guided renal mass biopsy is gaining increased diagnostic acceptance, but there are limited data concerning the safety and diagnostic yield of biopsy for small renal masses (≤4 cm). This study evaluated the safety, diagnostic yield, and management after image-guided percutaneous biopsy for small renal masses. METHODS: A retrospective IRB-approved study was conducted on patients who underwent renal mass biopsy for histopathologic diagnosis at a single center from 2015 to 2021...
February 19, 2024: Cancers
https://read.qxmd.com/read/38398177/use-of-droplet-digital-polymerase-chain-reaction-to-identify-biomarkers-for-differentiation-of-benign-and-malignant-renal-masses
#31
JOURNAL ARTICLE
Joshua P Hayden, Adam Wiggins, Travis Sullivan, Thomas Kalantzakos, Kailey Hooper, Alireza Moinzadeh, Kimberly Rieger-Christ
Several microRNAs (miRNAs) have been identified as cell-free biomarkers for detecting renal cell carcinoma (RCC). Droplet digital polymerase chain reaction (ddPCR) is a unique technology for nucleic acid quantification. It has the potential for superior precision, reproducibility, and diagnostic performance in identifying circulating miRNA biomarkers compared to conventional quantitative real-time PCR (qRT-PCR). This study aims to evaluate the performance of ddPCR compared to qRT- PCR in identifying miRNA biomarkers that differentiate malignant from benign renal masses...
February 15, 2024: Cancers
https://read.qxmd.com/read/38389212/renal-collision-tumor-a-case-of-small-cell-lung-cancer-metastasis-to-renal-angiomyolipoma
#32
JOURNAL ARTICLE
Aparna Singh, Hina J Shah, Borna E Dabiri, Wendy Landman
A 68-year-old woman presented with chest pain and shortness of breath. Imaging revealed a left hilar mass biopsy-proven as small cell cancer. Concurrently, a macroscopic fat-containing renal lesion consistent with an angiomyolipoma was observed. Systemic therapy achieved stability in the lungs and bones, and palliative radiation targeted the left hilum. However, progressive lung disease and brain metastases necessitated stereotactic radiosurgery for brain lesions. Notably, the renal angiomyolipoma exhibited increased soft tissue component and new focal uptake on FDG PET/CT...
February 23, 2024: Clinical Nuclear Medicine
https://read.qxmd.com/read/38388450/a-case-of-fat-forming-solitary-fibrous-tumor-that-is-prone-to-be-confused-with-liposarcoma
#33
JOURNAL ARTICLE
Yi-Dan Ma, Zi-Qing Wu, Xin-Rong Liang, Lin Jing Pi, Meng-Zhen Gong, Yao Tang
Fat-forming solitary fibrous tumor is a rare and specific subtype of solitary fibrous tumor. In this case, a mass of 8.3 cm in diameter was found in a 59-year-old male patient's right retroperitoneum, as revealed by abdominal contrast-enhanced computed tomography (CT) images. The tumor exhibited a well-circumscribed nature and histological features characterized by a combination of hemangiopericytomatous vasculature and mature adipose tissue, comprising around 70% of the total tumor composition. Immunohistochemistry staining revealed diffuse positive expression of STAT6 and CD34 in the tumor cells...
February 22, 2024: Diagnostic Pathology
https://read.qxmd.com/read/38374009/application-of-computed-tomography-scanning-parameters-combined-with-serum-cripto-1-in-the-diagnosis-of-renal-cell-carcinoma
#34
JOURNAL ARTICLE
Ning Liu, Chen Su, Jianghua Xue
OBJECTIVE: This study aims to analyse the clinical value of computed tomography (CT) scanning parameters combined with serum teratoma-derived growth factor-1 ( Cripto-1 ) in the diagnosis of renal cell carcinoma (RCC). METHODS: A retrospective analysis was conducted on 256 patients with renal tumour admitted to our hospital from July 2020 to December 2022. They were divided into malignant group (n = 180) and benign group (n = 76) based on the final pathological results...
January 2024: Archivos Españoles de Urología
https://read.qxmd.com/read/38335392/tuberous-sclerosis-complex-a-clinical-diagnosis-in-ethiopian-patients
#35
JOURNAL ARTICLE
Belete Sisay, Abilo Tadesse, Abebe Gelaw, Desalew Getahun, Biruk Mulat, Weynishet Kebede, Yonathan Gebrewold
RATIONALE: Tuberous sclerosis complex (TSC) is a rare autosomal dominant inherited disorder characterized by the development of nonmalignant tissue growths (hamartomas) in various organ systems, often located in the brain, skin, heart, lung and kidneys. The delayed diagnosis could be attributed to low expectation or exposure of physicians to this rare disease. High index of clinical suspicion is required for early diagnosis of rare diseases to prevent adverse outcomes. PATIENT CONCERNS: The first patient, a 27-year-old man, presented with intermittent left flank pain and hematuria of 5 months duration...
February 9, 2024: Medicine (Baltimore)
https://read.qxmd.com/read/38331445/platypnea-orthodeoxia-syndrome-pos-in-a-patient-who-had-undergone-partial-liver-resection
#36
JOURNAL ARTICLE
Bhavik Sandip Shah, Girish Ramkrishna Sabnis, Dhiraj Kumar, Charan Lanjewar
A South Asian male in his early 60s presented with acute-onset dyspnoea on postoperative day 4 after undergoing middle hepatic vein sacrificing partial liver resection for epithelioid angiomyolipoma. The patient's SpO2 on presentation was 65% in standing position which improved to 90% in left lateral decubitus. He was suspected of having platypnea-orthodeoxia syndrome (POS) which was confirmed on echocardiogram with microbubble contrast showing a large intracardiac right-to-left shunt. The patient was taken up for transcatheter closure of patent foramen ovale (PFO)...
February 7, 2024: BMJ Case Reports
https://read.qxmd.com/read/38327970/angiomyolipoma-with-epithelial-cysts-a-rare-but-distinct-variant-of-angiomyolipoma
#37
Vijai R, Pritam Sharma, Parth A Patel, Pratik Patil
Renal angiomyolipomas, common benign tumors, can exhibit slow growth in sporadic cases or have aggressive tendencies when linked to genetic conditions like tuberous sclerosis. This case report focuses on the exceptionally rare angiomyolipoma with epithelial cysts (AMLEC) variant, particularly challenging to diagnose due to its scarcity. Describing a 41-year-old woman's case, initially suspected to be renal cell carcinoma during an infertility evaluation, subsequent partial nephrectomy revealed a tumor comprising smooth muscle, blood vessels, and fat, with cystic regions featuring cuboidal linings and a layer devoid of abnormal cell activity...
January 2024: Curēus
https://read.qxmd.com/read/38327672/complications-of-lymphangioleiomyomatosis-in-pregnancy-a-case-report-and-review-of-the-literature
#38
Eileen Wang-Koehler, Adina R Kern-Goldberger, Sindhu K Srinivas
Lymphangioleiomyomatosis is a rare cystic lung disease primarily affecting premenopausal females and may be exacerbated by pregnancy. We conducted a literature review of lymphangioleiomyomatosis during pregnancy with a specific focus on related maternal morbidity and obstetrical outcomes. We also report a case of lymphangioleiomyomatosis that presented as an acute spontaneous pneumothorax in the third trimester of pregnancy, followed by significant maternal morbidity. A 37-year-old primigravid woman who presented at 29 weeks 5 days gestation with chest pain was diagnosed with spontaneous pneumothorax...
February 2024: AJOG global reports
https://read.qxmd.com/read/38320830/spontaneous-rupture-of-renal-angiomyolipoma-in-pregnancy-mimicking-preterm-labour
#39
JOURNAL ARTICLE
Nurul I Basri, Rima A Dasrilsyah
Ruptured renal angiomyolipoma in pregnancy is uncommon. Pregnant women may present with nonspecific symptoms such as flank or abdominal pain, contraction pain and haematuria. A thorough assessment is needed to reach the correct diagnosis. Management varies between conservative measures, radiological intervention or surgery depending on the patient's haemodynamic status and foetal condition. We present a case of a woman in her 30s, gravida 5 para 3+1 at 28 weeks of gestation, who presented with pain. The pain worsened, and she went into hypovolaemic shock...
February 6, 2024: BMJ Case Reports
https://read.qxmd.com/read/38312755/primary-renal-liposarcoma-simulating-angiomyolipoma
#40
Ryan C Rizk, Mohammad Yasrab, Linda C Chu, Edmund M Weisberg, Elliot K Fishman
Liposarcomas are infrequent malignant tumors of mesenchymal origin most commonly seen in the extremities. Although infrequent, these can develop as primary lesions in the soft tissue of the kidney, making them difficult to diagnose through imaging modalities alone. Primary renal liposarcomas are associated with poor prognoses, increasing the importance of timely and accurate diagnosis. In extremely rare instances, the tumor can arise directly from the fat in the epicenter of the kidney, disguised as an angiomyolipoma...
April 2024: Radiology Case Reports
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