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Article ; Online: Body Imaging: Past. Present. Future. The 2021

Elsayes, Khaled M / Katabathina, Venkata S / Luna, Antonio / Menias, Christine O

Radiographics : a review publication of the Radiological Society of North America, Inc

2021 Volume 41, Issue 6, Page(s) 1569

MeSH term(s)	Diagnostic Imaging ; Humans
Language	English
Publishing date	2021-10-13
Publishing country	United States
Document type	Editorial
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.2021210195
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Article ; Online: Factors Limiting Magnetic Resonance Imaging Diagnosis of Placenta Accreta Spectrum.

Cheng, CeCe / Ramsey, Patrick S / Byrne, John J / Katabathina, Venkata S / Ireland, Kayla E / Munoz, Jessian L

American journal of perinatology

2023 Volume 40, Issue 13, Page(s) 1398–1405

Abstract: Objective: Placenta accreta spectrum (PAS) disorders are characterized by an abnormal adherence of the placenta to the uterine myometrium. Magnetic resonance imaging (MRI) is an important adjunct in antenatal diagnosis. We sought to determine if there ... ...

Abstract	Objective: Placenta accreta spectrum (PAS) disorders are characterized by an abnormal adherence of the placenta to the uterine myometrium. Magnetic resonance imaging (MRI) is an important adjunct in antenatal diagnosis. We sought to determine if there are patient and MRI characteristics that limit the accuracy of PAS diagnosis and degree of invasion. Study design: We conducted a retrospective cohort analysis of patients who were evaluated for PAS by MRI from January 2007 to December 2020. Patient characteristics evaluated included number of prior cesarean deliveries, history of dilation and curettage (D&C) or dilation and evacuation (D&E), short interval pregnancy less than 18 months, and delivery body mass index (BMI). All patients were followed until delivery and MRI diagnosis was compared with final histopathology. Results: Of the 353 patients with suspected PAS, 152 (43%) underwent MRI evaluation and were included in the final analysis. In patients who underwent MRI evaluation, 105 (69%) had confirmed PAS on pathology. Patient characteristics were similar between groups and not associated with accuracy of MRI diagnosis. MRI was accurate in diagnosing PAS and the associated degree of invasion in 83 (55%) patients. Accuracy was associated with lacunae (8 vs. 0%, Conclusion: Patient factors did not change MRI accuracy of PAS diagnosis. MRI is associated with a significant overdiagnosis of PAS when dark T2 bands are present, and underdiagnose PAS when performed earlier in gestation or when lateral placentation is present. Key points: · Patient factors are not associated with MRI accuracy of PAS diagnosis.. · MRI overdiagnoses PAS invasion when there are dark T2 bands.. · MRI underdiagnoses PAS invasion when performed earlier in gestation.. · Underdiagnosis of PAS is associated with lateral placentation..
MeSH term(s)	Pregnancy ; Humans ; Female ; Placenta Accreta/pathology ; Retrospective Studies ; Placenta/diagnostic imaging ; Placenta/pathology ; Prenatal Diagnosis/methods ; Magnetic Resonance Imaging/methods
Language	English
Publishing date	2023-05-24
Publishing country	United States
Document type	Journal Article
ZDB-ID	605671-4
ISSN	1098-8785 ; 0735-1631
ISSN (online)	1098-8785
ISSN	0735-1631
DOI	10.1055/a-2099-4542
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Zs.A 1929: Show issues

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Article ; Online: Wunderlich Syndrome: Comprehensive Review of Diagnosis and Management.

Shah, Jignesh N / Gandhi, Darshan / Prasad, Srinivasa R / Sandhu, Preet K / Banker, Hiral / Molina, Ryan / Khan, Salman / Garg, Tushar / Katabathina, Venkata S

Radiographics : a review publication of the Radiological Society of North America, Inc

2023 Volume 43, Issue 6, Page(s) e220172

Abstract: Wunderlich syndrome (WS), which was named after Carl Wunderlich, is a rare clinical syndrome characterized by an acute onset of spontaneous renal hemorrhage into the subcapsular, perirenal, and/or pararenal spaces, without a history of antecedent trauma. ...

Abstract	Wunderlich syndrome (WS), which was named after Carl Wunderlich, is a rare clinical syndrome characterized by an acute onset of spontaneous renal hemorrhage into the subcapsular, perirenal, and/or pararenal spaces, without a history of antecedent trauma. Patients may present with a multitude of symptoms ranging from nonspecific flank or abdominal pain to serious manifestations such as hypovolemic shock. The classic symptom complex of flank pain, a flank mass, and hypovolemic shock referred to as the Lenk triad is seen in a small subset of patients. Renal neoplasms such as angiomyolipomas and clear cell renal cell carcinomas that display an increased proclivity for hemorrhage and rupture contribute to approximately 60%-65% of all cases of WS. A plethora of renal vascular diseases (aneurysms or pseudoaneurysms, arteriovenous malformations or fistulae, renal vein thrombosis, and vasculitis syndromes) account for 20%-30% of cases of WS. Rare causes of WS include renal infections, cystic diseases, calculi, kidney failure, and coagulation disorders. Cross-sectional imaging modalities, particularly multiphasic CT or MRI, are integral to the detection, localization, and characterization of the underlying causes and facilitate optimal management. However, large-volume hemorrhage at patient presentation may obscure underlying causes, particularly neoplasms. If the initial CT or MRI examination shows no contributary causes, a dedicated CT or MRI follow-up study may be warranted to establish the cause of WS. Renal arterial embolization is a useful, minimally invasive, therapeutic option in patients who present with acute or life-threatening hemorrhage and can help avoid emergency radical surgery. Accurate diagnosis of the underlying cause of WS is critical for optimal patient treatment in emergency and nonemergency clinical settings.
MeSH term(s)	Humans ; Follow-Up Studies ; Kidney Neoplasms/complications ; Kidney Neoplasms/diagnostic imaging ; Kidney Neoplasms/therapy ; Kidney/diagnostic imaging ; Hemorrhage/diagnostic imaging ; Hemorrhage/etiology ; Hemorrhage/therapy ; Shock
Language	English
Publishing date	2023-05-25
Publishing country	United States
Document type	Review ; Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.220172
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Article ; Online: Imaging of urachal anomalies.

Buddha, Suryakala / Menias, Christine O / Katabathina, Venkata S

Abdominal radiology (New York)

2019 Volume 44, Issue 12, Page(s) 3978–3989

Abstract: Urachal anomalies are classified into four types depending on the level of persistence of the embryonic urachal remnants between the urinary bladder and the umbilicus: patent urachus, umbilical-urachal sinus, urachal cyst, and vesico-urachal diverticulum. ...

Abstract	Urachal anomalies are classified into four types depending on the level of persistence of the embryonic urachal remnants between the urinary bladder and the umbilicus: patent urachus, umbilical-urachal sinus, urachal cyst, and vesico-urachal diverticulum. Due to the increasing use of cross-sectional imaging, urachal anomalies are frequently detected as incidental findings. Imaging plays a pivotal role in the initial diagnosis, evaluation of complications, treatment follow-up, and long-term surveillance of patients with urachal anomalies. Different urachal anomalies demonstrate characteristic imaging features that aid in a timely diagnosis and guide treatment. A patent urachus is visualized as an elongated tubular structure between the umbilicus and the urinary bladder. While umbilical-urachal sinus appears as focal dilatation at the umbilical end of the urachal remnant, the vesico-urachal diverticulum presents as a focal outpouching of the urinary bladder at anterosuperior aspect. Urachal cysts are identified as midline fluid-filled sacs most frequently located near the dome of the urinary bladder. Untreated urachal anomalies could progress into potential complications, including infection and malignancy. Knowledge regarding imaging features of urachal anomalies helps in timely diagnosis, treatment, follow-up, and early detection of complications.
MeSH term(s)	Contrast Media ; Diagnosis, Differential ; Humans ; Incidental Findings ; Urachus/abnormalities ; Urogenital Abnormalities/complications ; Urogenital Abnormalities/diagnostic imaging ; Urogenital Abnormalities/therapy
Chemical Substances	Contrast Media
Language	English
Publishing date	2019-09-02
Publishing country	United States
Document type	Journal Article ; Review
ZDB-ID	2839786-1
ISSN	2366-0058 ; 2366-004X
ISSN (online)	2366-0058
ISSN	2366-004X
DOI	10.1007/s00261-019-02205-x
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Article ; Online: Erratum for: Wunderlich Syndrome: Comprehensive Review of Diagnosis and Management.

Shah, Jignesh N / Gandhi, Darshan / Prasad, Srinivasa R / Sandhu, Preet K / Banker, Hiral / Molina, Ryan / Khan, Muhammad Salman / Garg, Tushar / Katabathina, Venkata S

Radiographics : a review publication of the Radiological Society of North America, Inc

2023 Volume 43, Issue 7, Page(s) e239007

Language	English
Publishing date	2023-06-29
Publishing country	United States
Document type	Published Erratum
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.239007
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Article ; Online: Morphomolecular Classification Update on Hepatocellular Adenoma, Hepatocellular Carcinoma, and Intrahepatic Cholangiocarcinoma.

Katabathina, Venkata S / Khanna, Lokesh / Surabhi, Venkateswar R / Minervini, Marta / Shanbhogue, Krishna / Dasyam, Anil K / Prasad, Srinivasa R

Radiographics : a review publication of the Radiological Society of North America, Inc

2022 Volume 42, Issue 5, Page(s) 1338–1357

Abstract: Hepatocellular adenomas (HCAs), hepatocellular carcinomas (HCCs), and intrahepatic cholangiocarcinomas (iCCAs) are a highly heterogeneous group of liver tumors with diverse pathomolecular features and prognoses. High-throughput gene sequencing techniques ...

Abstract	Hepatocellular adenomas (HCAs), hepatocellular carcinomas (HCCs), and intrahepatic cholangiocarcinomas (iCCAs) are a highly heterogeneous group of liver tumors with diverse pathomolecular features and prognoses. High-throughput gene sequencing techniques have allowed discovery of distinct genetic and molecular underpinnings of these tumors and identified distinct subtypes that demonstrate varied clinicobiologic behaviors, imaging findings, and complications. The combination of histopathologic findings and molecular profiling form the basis for the morphomolecular classification of liver tumors. Distinct HCA subtypes with characteristic imaging findings and complications include
MeSH term(s)	Adenoma, Liver Cell/genetics ; Adenoma, Liver Cell/pathology ; Bile Duct Neoplasms/diagnostic imaging ; Bile Duct Neoplasms/pathology ; Bile Ducts, Intrahepatic/metabolism ; Bile Ducts, Intrahepatic/pathology ; Carcinoma, Hepatocellular/diagnostic imaging ; Carcinoma, Hepatocellular/metabolism ; Cholangiocarcinoma/diagnostic imaging ; Cholangiocarcinoma/pathology ; Hedgehog Proteins/metabolism ; Humans ; Liver Neoplasms/diagnostic imaging ; Liver Neoplasms/pathology ; beta Catenin/genetics
Chemical Substances	Hedgehog Proteins ; beta Catenin
Language	English
Publishing date	2022-07-01
Publishing country	United States
Document type	Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.210206
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Article ; Online: Mesenchymal Neoplasms of the Prostate and Seminal Vesicles: Spectrum of Disease with Radiologic-Pathologic Correlation.

Marcal, Leonardo P / Surabhi, Venkateswar R / Ramani, Nisha S / Katabathina, Venkata S / Paspulati, Raj M / Prasad, Srinivasa R

Radiographics : a review publication of the Radiological Society of North America, Inc

2022 Volume 42, Issue 2, Page(s) 417–432

Abstract: There is a wide spectrum of benign and malignant mesenchymal neoplasms of the prostate, which account for less than 1% of all prostatic tumors. These include distinctive tumors that arise from the specialized prostatic stroma and site-agnostic neoplasms ... ...

Abstract	There is a wide spectrum of benign and malignant mesenchymal neoplasms of the prostate, which account for less than 1% of all prostatic tumors. These include distinctive tumors that arise from the specialized prostatic stroma and site-agnostic neoplasms such as smooth muscle tumors, fibrous or myofibroblastic neoplasms, neurogenic tumors, vascular tumors, and a plethora of sarcomas. Select tumors show classic sites of origin within the prostate. While stromal tumors of uncertain malignant potential (STUMPs) commonly involve the peripheral zone at the prostate base, leiomyomas typically originate from the central prostate toward the apex. Some "prostatic" neoplasms such as gastrointestinal stromal tumors, solitary fibrous tumor (SFT), paragangliomas, and neurogenic tumors arise primarily from periprostatic soft tissues. Most mesenchymal tumors of the prostate and seminal vesicles manifest as large tumors that cause nonspecific symptoms; prostate-specific antigen level is not typically elevated. Diverse mesenchymal neoplasms demonstrate characteristic histopathologic and immunocytochemical features and variable cross-sectional imaging findings. While leiomyoma and SFT typically display low signal intensity on T2-weighted images, synovial sarcomas commonly show hemorrhage. Diagnosis is difficult because of the rarity and lack of awareness of the tumors and the significant overlap in histopathologic features. Select tumors show characteristic genetic abnormalities that allow the diagnosis to be established. For example, more than 90% of SFTs are characterized by a unique
MeSH term(s)	Biomarkers, Tumor/genetics ; Diagnosis, Differential ; Humans ; Male ; Neoplasm Recurrence, Local ; Prostate/diagnostic imaging ; Prostate/pathology ; Seminal Vesicles/diagnostic imaging ; Seminal Vesicles/pathology ; Solitary Fibrous Tumors/pathology
Chemical Substances	Biomarkers, Tumor
Language	English
Publishing date	2022-01-14
Publishing country	United States
Document type	Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.210084
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Reproducibility and Repeatability of Intravoxel Incoherent Motion MRI Acquisition Methods in Liver.

Vasquez, Juan A / Brown, Marissa / Woolsey, Mary / Abdul-Ghani, Mohammad / Katabathina, Venkata / Deng, Shengwen / Blangero, John / Clarke, Geoffrey D

Journal of magnetic resonance imaging : JMRI

2024

Abstract: Background: Intravoxel incoherent motion (IVIM) diffusion weighted MRI (DWI) has potential for evaluating hepatic fibrosis but image acquisition technique influence on diffusion parameter estimation bears investigation.: Purpose: To minimize ... ...

Abstract	Background: Intravoxel incoherent motion (IVIM) diffusion weighted MRI (DWI) has potential for evaluating hepatic fibrosis but image acquisition technique influence on diffusion parameter estimation bears investigation. Purpose: To minimize variability and maximize repeatably in abdominal DWI in terms of IVIM parameter estimates. Study type: Prospective test-retest and image quality comparison. Subjects: Healthy volunteers (3F/7M, 29.9 ± 12.9 years) and Family Study subjects (18F/12M, 51.7 ± 16.7 years), without and with liver steatosis. Field strength/sequence: Abdominal single-shot echo-planar imaging (EPI) and simultaneous multi-slice (SMS) DWI sequences with respiratory triggering (RT), breath-holding (BH), and navigator echo (NE) at 3 Tesla. Assessment: SMS-BH, EPI-NE, and SMS-RT data from twice-scanned healthy volunteers were analyzed using 6 × b-values (0-800 s⋅mm Statistical tests: Coefficients of variation (CoV) and Bland Altman analyses were performed for test-retest repeatability. Interclass correlation coefficient (ICC) assessed interobserver agreement with P < 0.05 deemed significant. Results: Within-subject CoVs among volunteers (N = 10) for f and D Data conclusion: Simultaneous multislice acquisitions had significantly less variability and higher ICCs of D Evidence level: 2 TECHNICAL EFFICACY: Stage 1.
Language	English
Publishing date	2024-01-19
Publishing country	United States
Document type	Journal Article
ZDB-ID	1146614-5
ISSN	1522-2586 ; 1053-1807
ISSN (online)	1522-2586
ISSN	1053-1807
DOI	10.1002/jmri.29249
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Zs.A 3648: Show issues			Location: Je nach Verfügbarkeit (siehe Angabe bei Bestand) bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular Jg. 1995 - 2021: Lesesall (2.OG) ab Jg. 2022: Lesesaal (EG)
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Article ; Online: Tuberous Sclerosis: Current Update.

Wang, Mindy X / Segaran, Nicole / Bhalla, Sanjeev / Pickhardt, Perry J / Lubner, Meghan G / Katabathina, Venkata S / Ganeshan, Dhakshinamoorthy

Radiographics : a review publication of the Radiological Society of North America, Inc

2021 Volume 41, Issue 7, Page(s) 1992–2010

Abstract: Tuberous sclerosis complex (TSC) is a relatively rare autosomal dominant neurocutaneous disorder secondary to mutations in ... ...

Abstract	Tuberous sclerosis complex (TSC) is a relatively rare autosomal dominant neurocutaneous disorder secondary to mutations in the
MeSH term(s)	Angiomyolipoma ; Carcinoma, Renal Cell ; Humans ; Kidney Neoplasms ; Lymphangioleiomyomatosis ; Tuberous Sclerosis/diagnostic imaging
Language	English
Publishing date	2021-09-17
Publishing country	United States
Document type	Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.2021210103
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Article ; Online: Mesotheliomas and Benign Mesothelial Tumors: Update on Pathologic and Imaging Findings.

Bonde, Apurva / Singh, Ramandeep / Prasad, Srinivasa R / Kamireddy, Dhiraj / Aggarwal, Aarushi / Ramani, Nisha / Saboo, Sachin / Shanbhogue, Krishna / Dasyam, Anil K / Katabathina, Venkata S

Radiographics : a review publication of the Radiological Society of North America, Inc

2023 Volume 43, Issue 3, Page(s) e220128

Abstract: A diverse spectrum of benign entities and malignant neoplasms originate from the monotonous mesothelium that lines the serosal membranes of the pleural, pericardial, and peritoneal cavities. The mesothelium of myriad sites shows a common origin from the ... ...

Abstract	A diverse spectrum of benign entities and malignant neoplasms originate from the monotonous mesothelium that lines the serosal membranes of the pleural, pericardial, and peritoneal cavities. The mesothelium of myriad sites shows a common origin from the lateral plate mesoderm; primary mesothelial tumors thus demonstrate similar pathogenesis, imaging findings, and treatment options. Significant changes have been made in the 2021 World Health Organization (WHO) classification schemata of the pleural and pericardial tumors on the basis of recent advances in pathology and genetics. While malignant mesotheliomas are biologically aggressive malignancies that occur primarily in patients exposed to asbestos with attendant poor survival rates, well-differentiated papillary mesothelial tumors and adenomatoid tumors charter a benign clinical course with an excellent prognosis. Mesothelioma in situ is a newly characterized entity represented by recurrent unexplained pleural effusions without any identifiable mass at imaging or thoracoscopy. Immunohistochemical markers based on
MeSH term(s)	Humans ; Adenomatoid Tumor ; Positron Emission Tomography Computed Tomography ; Mesothelioma/diagnostic imaging ; Mesothelioma/therapy ; Mesothelioma, Malignant ; Pleural Neoplasms/pathology ; Neoplasms, Mesothelial ; Biomarkers, Tumor
Chemical Substances	Biomarkers, Tumor
Language	English
Publishing date	2023-02-09
Publishing country	United States
Document type	Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.220128
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