CRP-34: Difference between revisions - Pathology Education Instructional Resource

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'''CRP-34'''

==Clinical History==

The patient is a 23 year old male with history of end-stage renal disease secondary to IgA nephropathy. Status post living related donor transplant. Creatinine has increased from 1.8 to 3.0. Hematuria, but no proteinuria.

==Gross Description:==

==Gross Description==

Received in transport media are two cores measuring 16 mm and 15 mm in length and 0.5 mm in diameter. Two 1-mm pieces are taken for EM, a 15-mm piece is submitted for immunofluorescence, and the remainder is submitted for light microscopy.

==Pathology==

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<peir-vm>specialcrp/CRP-034_Silver</peir-vm>

<div class="usermessage mw-customtoggle-diagnosis" style="cursor:pointer"> Microscopic Description, Immunofluorescence, and Electron Microscopy.</div>

<div class="usermessage mw-customtoggle-diagnosis" style="cursor:pointer"> Microscopic Description, Immunofluorescence, and Electron Microscopy</div>

==Microscopic Description:==

==Microscopic Description==

===Light Microscopy:===

===Light Microscopy===

The specimen consists of two fragments of renal cortex, one of which has a small piece of capsule on one end. The other fragment has a very tiny portion of medulla on one end. There are sixteen glomeruli in the three levels. None of these are obsolete, and none show segmental sclerosis. There is focal mild increase in mesangial matrix, but there is no hypercellularity. The capillary basement membranes are unremarkable with the silver and PASH stains. There is mild focal fibrosis with corresponding focal tubular atrophy. There is also interstitial edema, and a number of mononuclear inflammatory cells are present throughout the cortex. These are primarily lymphocytes with occasional eosinophils. Tubulitis is easily identified, although the most severely involved tubules contain less than ten lymphocytes per cross-section. Arterioles show mild thickening, but there is no arteritis

===Immunofluorescence:===

===Immunofluorescence===

There are four glomeruli in the sections. There is 1+ granular mesangial staining for IgM, but there is no glomerular staining for IgG, IgA, Clq, C3 or light chains. Blood vessels show 1+ staining for C3, and there is also focal staining for C3 in tubular epithelial cells. There is no staining of the tubular basement membranes.

~~===Electron Microscopy:===~~

===Electron Microscopy===

Two thick section are available, and each contains one glomerulus. These are similar to those described above and show essentially normal morphology. Ultrastructural examination reveals mild thickening of the capillary basement membranes, and there is focal fusion of the epithelial foot processes. No electron dense deposits are identified in the glomeruli.

</div></div>

Kidney, transplant, needle. biopsy - Mild acute interstitial rejection, Banff Grade I.

</spoiler>

@@ Line 1: / Line 1: @@
 '''CRP-34'''
 ==Clinical History==
+The patient is a 23 year old male with history of end-stage renal disease secondary to IgA nephropathy. Status post living related donor transplant. Creatinine has increased from 1.8 to 3.0. Hematuria, but no proteinuria.
-==Gross Description:==
+==Gross Description==
+Received in transport media are two cores measuring 16 mm and 15 mm in length and 0.5 mm in diameter. Two 1-mm pieces are taken for EM, a 15-mm piece is submitted for immunofluorescence, and the remainder is submitted for light microscopy.
 ==Pathology==
@@ Line 12: / Line 14: @@
 <peir-vm>specialcrp/CRP-034_Silver</peir-vm>
-<div class="usermessage mw-customtoggle-diagnosis" style="cursor:pointer"> Microscopic Description, Immunofluorescence, and Electron Microscopy.</div>
+<div class="usermessage mw-customtoggle-diagnosis" style="cursor:pointer"> Microscopic Description, Immunofluorescence, and Electron Microscopy</div>
 <div class="mw-collapsible mw-collapsed" id="mw-customcollapsible-diagnosis">
 <div class="mw-collapsible-content">
-==Microscopic Description:==
+==Microscopic Description==
-===Light Microscopy:===
+===Light Microscopy===
+The specimen consists of two fragments of renal cortex, one of which has a small piece of capsule on one end.  The other fragment has a very tiny portion of medulla on one end.  There are sixteen glomeruli in the three levels.  None of these are obsolete, and none show segmental sclerosis.  There is focal mild increase in mesangial matrix, but there is no hypercellularity.  The capillary basement membranes are unremarkable with the silver and PASH stains. There is mild focal fibrosis with corresponding focal tubular atrophy. There is also interstitial edema, and a number of mononuclear inflammatory cells are present throughout the cortex.  These are primarily lymphocytes with occasional eosinophils. Tubulitis is easily identified, although the most severely involved tubules contain less than ten lymphocytes per cross-section. Arterioles show mild thickening, but there is no arteritis
-===Immunofluorescence:===
+===Immunofluorescence===
+There are four glomeruli in the sections. There is 1+ granular mesangial staining for IgM, but there is no glomerular staining for IgG, IgA, Clq, C3 or light chains. Blood vessels show 1+ staining for C3, and there is also focal staining for C3 in tubular epithelial cells. There is no staining of the tubular basement membranes.
-===Electron Microscopy:===
+===Electron Microscopy===
+Two thick section are available, and each contains one glomerulus. These are similar to those described above and show essentially normal morphology. Ultrastructural examination reveals mild thickening of the capillary basement membranes, and there is focal fusion of the epithelial foot processes. No electron dense deposits are identified in the glomeruli.
 </div></div>
 <spoiler text="Diagnosis and Comments">
+Kidney, transplant, needle. biopsy - Mild acute interstitial rejection, Banff Grade I.
 </spoiler>