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Arkana Laboratories

@arkanalabs

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Arkana Laboratories is a center for esoteric pathology focused on one thing: improving care for patients.

Little Rock, AR
Joined September 2012
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@arkanalabs
Arkana Laboratories
7 months
Looking for a new specialty? Explore the world of kidneys at Arkana Labs with our specialized mid-career transition program. Join a highly supportive and collaborative team focused on improving patient care. Learn more:
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@arkanalabs
Arkana Laboratories
32 minutes
What is your diagnosis? #DiagnoseThis #renalpath #nephropath
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@arkanalabs
Arkana Laboratories
4 days
Today's #eyeSCANdy is an acellular scanning EM showing glomerular basement membrane duplication at high power in a glomerulus with a membranoproliferative pattern of injury.  Photo courtesy of Dr. Stephen Bonsib. #renal #pathology
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@arkanalabs
Arkana Laboratories
5 days
A sample from the pathology teaching slide set on Anti-glomerular Basement Membrane (Anti-GBM) Antibody Glomerulonephritis, jointly prepared by Arkana Laboratories and @goKDIGO. #KDIGO #renalpath #kidneypath
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@arkanalabs
Arkana Laboratories
6 days
@arkanalabs
Arkana Laboratories
6 days
This photomicrograph (PAS stain) shows a glomerulus with mesangial expansion by an acellular, PAS-pale, homogenous material consistent with amyloid. Further confirmation staining by Congo red shows positive staining within areas of amyloid deposition and apple-green birefringence on polarization. By immunofluorescence the amyloid deposits showed lambda light chain restriction making this an AL-type amyloidosis. #nephropath #renalpath
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@arkanalabs
Arkana Laboratories
6 days
This photomicrograph (PAS stain) shows a glomerulus with mesangial expansion by an acellular, PAS-pale, homogenous material consistent with amyloid. Further confirmation staining by Congo red shows positive staining within areas of amyloid deposition and apple-green birefringence on polarization. By immunofluorescence the amyloid deposits showed lambda light chain restriction making this an AL-type amyloidosis. #nephropath #renalpath
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@arkanalabs
Arkana Laboratories
7 days
What is your diagnosis? #DiagnoseThis #renalpath #nephropath
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@arkanalabs
Arkana Laboratories
6 days
The silver impregnation stain is a key method of identifying basement membranes in human tissue, and its application in renal pathology is nearly universal. Notice in this image (Fig 1) how clearly demonstrating the capillary basement membrane using the silver stain allows one to distinguish cells within the capillary lumens from those “extracapillary” cells which are forming the glomerular crescent. In 1951, David B. Jones, MD, reported the development of a periodic acid silver reaction adapted specifically for the kidney which better highlighted basement membranes (American Journal of Pathology, Dec 1951: 991-1009). Most renal pathologists still rely heavily on the Jones stain in their daily diagnostic pathology practice and are grateful to the many contributions made by Dr. Jones to the field of renal pathology (Fig 2). #TeachingPoints #kidneypath #renal
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@arkanalabs
Arkana Laboratories
10 days
ANSWER: B The target of the circulating ABBA autoantibodies is LDL receptor-related protein 2 (LRP2) also known as “Megalin”. ABBA is a rare autoimmune disease associated with acute kidney injury and tubulointerstitial damage. Histologically, IgG–positive immune deposits are found in tubular basement membranes by immunofluorescence (IF). When indirect IF is done using patient’s serum and normal kidney controls, there is reaction of the autoantibodies with the proximal tubular brush borders. REFERENCE: Larsen CP, et al. LDL-Receptor Related Protein 2 (Megalin) as a Target Antigen in Human Kidney Anti-Brush Border Antibody Disease. J Am Soc Nephrol, 2018; 29:644-653
@arkanalabs
Arkana Laboratories
11 days
#PathQuiz What is the name of the target antigen in anti-brush border antibody (ABBA) disease?
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@arkanalabs
Arkana Laboratories
11 days
#PathQuiz What is the name of the target antigen in anti-brush border antibody (ABBA) disease?
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@arkanalabs
Arkana Laboratories
11 days
RT @nephrosharma: Register now !
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@arkanalabs
Arkana Laboratories
11 days
Today's #eyeSCANdy is an acellular scanning EM showing glomerular basement membrane duplication from a glomerulus with a membranoproliferative pattern of injury.   Photo courtesy of Dr. Stephen Bonsib. #renal #pathology
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@arkanalabs
Arkana Laboratories
12 days
A sample from the pathology teaching slide set on Lupus Nephritis, jointly prepared by Arkana Laboratories and @goKDIGO. #KDIGO #renalpath #kidneypath
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@arkanalabs
Arkana Laboratories
13 days
@arkanalabs
Arkana Laboratories
13 days
The correct answer is Eosinophilic vasculitis. Read more here:
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@arkanalabs
Arkana Laboratories
13 days
The correct answer is Eosinophilic vasculitis. Read more here:
@arkanalabs
Arkana Laboratories
14 days
The patient is a 62-year-old woman with asthma, GERD, moderate alcohol intake, and hypertension who presents with 4 weeks of weakness, arthralgia, and fatigue. Her family history is significant for breast cancer and alcohol abuse. She has been treated initially with prednisone with only mild improvement. Her lab results show a highest CK of 1582, alkaline phosphatase of 121, CRP of 35.9, and an absolute eosinophilia.  What is the diagnosis? #DiagnoseThis #NeuroNotes #neuropath #neuromuscular
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@arkanalabs
Arkana Laboratories
13 days
@arkanalabs
Arkana Laboratories
13 days
The photomicrograph is a high power PAS-stained section showing a glomerulus with focal segmental glomerulosclerosis, tip-lesion type. At 10 o'clock you can see a capillary loop becoming adherent to the take-off of the proximal tubule which also shows endocapillary foam cell formation and extracapillary protein resorption droplets. While the findings in this case are a bit more subtle than some, these are classic findings for focal segmental glomerulosclerosis, tip lesion type. This patient presented with abrupt onset of nephrotic syndrome and nephrotic range proteinuria with no significant past history of kidney disease. Clinically, focal segmental glomerulosclerosis, tip lesion type has the most favorable prognosis of all forms of focal segmental glomerulosclerosis and is frequently corticosteroid responsive. #nephropath #renalpath
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@arkanalabs
Arkana Laboratories
13 days
The photomicrograph is a high power PAS-stained section showing a glomerulus with focal segmental glomerulosclerosis, tip-lesion type. At 10 o'clock you can see a capillary loop becoming adherent to the take-off of the proximal tubule which also shows endocapillary foam cell formation and extracapillary protein resorption droplets. While the findings in this case are a bit more subtle than some, these are classic findings for focal segmental glomerulosclerosis, tip lesion type. This patient presented with abrupt onset of nephrotic syndrome and nephrotic range proteinuria with no significant past history of kidney disease. Clinically, focal segmental glomerulosclerosis, tip lesion type has the most favorable prognosis of all forms of focal segmental glomerulosclerosis and is frequently corticosteroid responsive. #nephropath #renalpath
@arkanalabs
Arkana Laboratories
14 days
What is your diagnosis? #DiagnoseThis #renalpath #nephropath
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@arkanalabs
Arkana Laboratories
13 days
A very common vascular histologic finding in patients with hypertensive nephrosclerosis is arteriosclerosis. In advanced lesions, such as this example, there is prominent intimal fibrosis with narrowing of the vessel lumen. The replacement of smooth muscle cells in the tunica media by fibrous tissue is thought to result from collagen and elastic tissue synthesis by myointimal cells. The degree of intimal fibrosis is thought to be more closely associated with elevated blood pressure than the degree of hyaline arteriolosclerosis. #TeachingPoints #kidneypath #renal
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@arkanalabs
Arkana Laboratories
17 days
ANSWER: B The medulla is the only compartment affected by AAPOAIV amyloidosis, sometimes with large amounts of amyloid. Glomeruli and vessels are spared and not affected by this type of amyloid. AAPOAIV Amyloidosis is a systemic amyloidosis reported from wild-type apolipoprotein AIV. When the kidney is involved the patient presents with gradual loss of renal function and proteinuria. It may also have cardiac involvement. References: Sethi S, Theis JD, Shiller SM, et al. Medullary amyloidosis associated with apolipoprotein A-IV deposition. Kidney Int 81: 201–206, 2012. Dasari S, Amin S, Kurtin P, et al. Clinical, biopsy, and mass spectrometry characteristics of renal apolipoprotein A-IV amyloidosis. Kidney Int 90: 658-64, 2016.
@arkanalabs
Arkana Laboratories
18 days
#PathQuiz Amyloid derived from apolipoprotein IV (AAPOAIV) in the kidney usually involves:
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