CRP-17 - Revision history

Peter Anderson at 14:26, 8 October 2026

2026-10-08T14:26:39Z

← Older revision		Revision as of 09:26, 8 October 2026
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	<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>
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Peter Anderson at 20:41, 7 October 2026

2026-10-07T20:41:49Z

← Older revision		Revision as of 15:41, 7 October 2026
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	'''CRP-017'''		'''CRP-017'''
	==Clinical History==		==Clinical History==
			The patient is a 72 year old male. Acute renal failure of unknown etiology. Creatinine 5.5, BUN 75, urinary protein 371 mg/day. Normal complements, ANA, RA and SPEP. Patient has recently taken some Advil, but exact amount is unknown. Urinalysis shows 10 to 15 RBCs per high powered field, broad granular casts and no cellular casts.

	==Gross Description:==		==Gross Description==
			Received in saline are six cores measuring 6, 7, 12, 14, 10 and 14 mm in length and 1 mm in diameter. Four 1-mm pieces are taken for electron microscopy. Three cores measuring 12, 13 and 8 mm in length are submitted for immunofluorescence, and the remaining tissue is submitted for light microscopy.

	==Pathology==		==Pathology==
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	==Microscopic Description:==		==Microscopic Description==
	===Light Microscopy:===		===Light Microscopy===
			The specimen consists of three fragments of renal cortex that contain fifteen glomeruli in the three levels. None of these are obsolete, and none show segmental sclerosis. The glomeruli generally appear atrophic with thickened and wrinkled capillary basement membranes. However, two glomeruli demonstrate segmental necrosis ac the vascular pole, probably representing vasculitis of the afferent arteriole. There are no cellular or fibrous crescents. The PASH and trichrome stains show diffuse moderately severe interstitial fibrosis and tubular atrophy. There is tremendous acute interstitial inflammation. Most of the cells are polymorphonuclear leukocytes with a small percentage of eosinophils. This is associated with numerous examples of mild tubulitis. The most striking feature of the biopsy is the large vessels. Several show transmural inflammation with severe fibrinoid necrosis. Some of the vessels show rupture into the adjacent parenchyma, which is accompanied by severe interstitial inflammation. The arterioles are mildly thickened but are otherwise unremarkable.

	===Immunofluorescence:===		===Immunofluorescence===
			There are eleven glomeruli in the sections. None of these contain crescents. There is 1+ focal and segmental mesangial staining for IgM, Clq and C3. There is no glomerular staining for IgG, IgA, albumin or light chains. There is no staining of the tubular basement membranes or vessels. There is focal staining for C3 in Bowman's capsule.

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

			===Electron Microscopy===
			Three thick sections containing a total of two glomeruli are available. Ultrastructural examination of these two glomeruli reveals focal thickening and wrinkling of the glomerular basement membranes. The subendothelial space is widened and filled with pale, loose granular material. There is mild increase in mesangial matrix. The epithelial cell foot processes are completely effaced. No electron dense deposits are identified.

	</div></div>		</div></div>

	<spoiler text="Diagnosis and Comments">		<spoiler text="Diagnosis and Comments">
			Kidney, needle biopsy - Polyarteritis nodosa.

			These features are most consistent with polyarteritis nodosa (macroscopic polyarteritis). This lesion is distinctly different from microscopic polyangiitis. In particular, ANCA serology is rarely positive in polyarteritis nodosa, and glomerulonephritis is rare. On the other hand, there are typically ischemic glomerular lesions, such as those described in this biopsy. Unfortunately, there is already moderately severe tubulointerstitial scarring. This scarring, in association with the severe necrotizing vasculitis, suggests that significant recovery of renal function is very unlikely.

	</spoiler>		</spoiler>

Peter Anderson: Created page with "'''CRP-017''' ==Clinical History== ==Gross Description:== ==Pathology== ===Case CRP-017 H&E=== specialcrp/CRP-017_HE ===Case CRP-017 PASH=== specialcrp/CRP-017_PASH ===Case CRP-017 Silver=== specialcrp/CRP-017_Silver
Microscopic Description, Immunofluorescence, and Electron Microscopy.

2026-10-07T17:33:42Z

Created page with "'''CRP-017''' ==Clinical History== ==Gross Description:== ==Pathology== ===Case CRP-017 H&E=== <peir-vm>specialcrp/CRP-017_HE</peir-vm> ===Case CRP-017 PASH=== <peir-vm>specialcrp/CRP-017_PASH</peir-vm> ===Case CRP-017 Silver=== <peir-vm>specialcrp/CRP-017_Silver</peir-vm> <div class="usermessage mw-customtoggle-diagnosis" style="cursor:pointer"> Microscopic Description, Immunofluorescence, and Electron Microscopy.</div> <div class="mw-collapsible mw-collapsed" id="mw..."

New page
'''CRP-017'''
==Clinical History==

==Gross Description:==

==Pathology==
===Case CRP-017 H&E===
<peir-vm>specialcrp/CRP-017_HE</peir-vm>
===Case CRP-017 PASH===
<peir-vm>specialcrp/CRP-017_PASH</peir-vm>
===Case CRP-017 Silver===
<peir-vm>specialcrp/CRP-017_Silver</peir-vm>

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

==Microscopic Description:==
===Light Microscopy:===

===Immunofluorescence:===

===Electron Microscopy:===

</div></div>

<spoiler text="Diagnosis and Comments">

</spoiler>