Case 6.2

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

72-year-old man with a history of autoimmune hemolytic anemia and recurrent fevers of unknown origin presenting with new right flank pain Coronal SSFSE (Figure 6.2.1) and axial fat-suppressed T2-weighted FSE images (Figure 6.2.2) demonstrate a lenticular right adrenal lesion with a hyperintense outer margin. Diffusion-weighted image (b=600 s/mm...

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

72-year-old man with left flank pain and a history of bleeding diathesis, for which he takes warfarin Axial FSE T2-weighted image (Figure 7.29.1) reveals a posterior left perinephric mass with heterogeneous increased signal intensity. Axial diffusion- weighted image (b=800 s/mm2) and the corresponding ADC map (...


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

46-year-old woman with history of appendiceal goblet cell carcinoid, resected 3 years previously, who underwent MRI to assess for hepatic metastases Axial fat-suppressed FSE T2-weighted images (Figure 11.18.1) and sagittal fat-suppressed 2D SSFP image (Figure 11.18.2) reveal a large, mildly heterogeneous mass in the central pelvis superior to the uterus with diffusely high signal intensity and a few scattered cystic components. Axial diffusion-weighted image (b=800 s/mm...


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

57-year-old man with a history of alcoholic cirrhosis Axial fat-suppressed FSE T2-weighted (Figure 1.24.1) and diffusion-weighted (b=100 s/mm2) (Figure 1.24.2) images demonstrate a peripheral right hepatic lobe mass that has mildly increased signal intensity relative to adjacent liver. Notice the higher signal intensity and greater contrast on the diffusion-weighted image (b=100 s/mm...


2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Gurchetan Randhawa ◽  
Chia-Yu Chiu ◽  
Thanunthorn Suban Na Ayutthaya

Autoimmune hemolytic anemia (AIHA) can be caused by a variety of etiologies. AIHA is associated with the development of coagulopathy, leading to potentially fatal pulmonary emboli. Here, we present a case of a 66-year-old female with a past medical history of non-Hodgkin’s lymphoma and gastritis treated with triple therapy that developed warm AIHA. The patient later succumbed to a suspected pulmonary embolus.


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

68-year-old man with a history of prostatectomy for prostate adenocarcinoma, increasing nocturnal urinary frequency, and rising PSA level Sagittal FSE T2-weighted image (Figure 8.17.1) obtained using an endorectal coil shows a large lobulated mass in the posterior bladder wall extending superiorly to the dome and inferiorly to the vesicourethral junction. The mass has high signal intensity on an axial diffusion-weighted image (b=1,000 s/mm...


1995 ◽  
Vol 6 (3) ◽  
pp. 300-301 ◽  
Author(s):  
J.C. Byrd ◽  
A.A. Hertler ◽  
R.B. Weiss ◽  
J. Freiman ◽  
S.L. Kweder ◽  
...  

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

72-year-old man with a history of prostate cancer and new posterior right buttock pain Axial (Figure 14.1.1) and coronal oblique (Figure 14.1.2) T1-weighted images and axial (Figure 14.1.3) and coronal oblique (Figure 14.1.4) fat-suppressed T2-weighted FSE images demonstrate a linear defect in the right side of the sacrum with low signal intensity on T1-weighted images and mildly increased T2-signal intensity. Axial diffusion-weighted image (b=800 s/mm...


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

22-year-old woman with a history of diabetes mellitus, hyperlipidemia, and polycystic ovarian syndrome; she was involved in a motor vehicle accident, and abdominal CT demonstrated multiple hepatic masses Axial fat-suppressed FSE T2-weighted image (Figure 1.16.1) demonstrates at least 2 hyperintense masses in the periphery of the right hepatic lobe. Diffusion-weighted image (b=600 s/mm...


2018 ◽  
Vol 7 (9) ◽  
pp. 230
Author(s):  
Deng-Ho Yang ◽  
Meng-Yin Yang

Evans syndrome is a rare disorder with presentations of autoimmune hemolytic anemia and immune thrombocytopenia, in the absence of any underlying cause. Here, we reported a case with a history of Evans syndrome for seven years. A persistent scrotal ulcer with severe pain occurred for two weeks. He called at our emergency room because of a painful, necrolytic cutaneous ulcer over the scrotal region. A biopsy showed sterile dermal neutrophilia with lymphocytic vasculitis, and pyoderma gangrenosum was impressed. The patient received steroid treatment and recovery after one month.


2020 ◽  
Vol 59 (13) ◽  
pp. 1209-1213
Author(s):  
Ashley Gureck ◽  
Zina McSweeney ◽  
Mandolin Ziadie ◽  
Robert J. Casey ◽  
Alexandru R. Constantinescu

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