出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/12/01 20:58:17」(JST)
Urinary casts are cylindrical structures produced by the kidney and present in the urine in certain disease states. They form in the distal convoluted tubule and collecting ducts of nephrons, then dislodge and pass into the urine, where they can be detected by microscopy.
They form via precipitation of Tamm-Horsfall mucoprotein which is secreted by renal tubule cells, and sometimes also by albumin in conditions of proteinuria. Cast formation is pronounced in environments favoring protein denaturation and precipitation (low flow, concentrated salts, low pH). Tamm-Horsfall protein is particularly susceptible to precipitation in these conditions.
Casts were first described by Henry Bence Jones (1813-1873).[1]
As reflected in their cylindrical form, casts are generated in the small distal convoluted tubules and collecting ducts of the kidney, and generally maintain their shape and composition as they pass through the urinary system. Although the most common forms are benign, others indicate disease. All rely on the inclusion or adhesion of various elements on a mucoprotein base—the hyaline cast. "Cast" itself merely describes the shape, so an adjective is added to describe the composition of the cast. Various casts found in urine sediment may be classified as follows.
The most common type of cast, hyaline cast are solidified Tamm-Horsfall mucoprotein secreted from the tubular epithelial cells of individual nephrons. Low urine flow, concentrated urine, or an acidic environment can contribute to the formation of hyaline casts, and, as such, they may be seen in normal individuals in dehydration or vigorous exercise. Hyaline casts are cylindrical and clear, with a low refractive index, so that they can easily be missed on cursory review under brightfield microscopy, or in an aged sample where dissolution has occurred. On the other hand, phase contrast microscopy leads to easier identification. Given the ubiquitous presence of Tamm-Horsfall protein, other cast types are formed via the inclusion or adhesion of other elements to the hyaline base.
The second-most common type of cast, granular casts can result either from the breakdown of cellular casts or the inclusion of aggregates of plasma proteins (e.g., albumin) or immunoglobulin light chains. Depending on the size of inclusions, they can be classified as fine or coarse, though the distinction has no diagnostic significance. Their appearance is generally more cigar-shaped and of a higher refractive index than hyaline casts. While most often indicative of chronic renal disease, these casts, as with hyaline casts, can also be seen for a short time following strenuous exercise.[2] The "muddy brown cast" seen in acute tubular necrosis is a type of granular cast.
Thought to represent the end product of cast evolution, waxy casts suggest the very low urine flow associated with severe, longstanding kidney disease such as renal failure. Additionally, due to urine stasis and their formation in diseased, dilated ducts, these casts are significantly larger than hyaline casts. They are cylindrical. They possess a higher refractive index. They are more rigid, demonstrating sharp edges, fractures, and broken-off ends. Waxy casts are broad casts. a more general term to describe the wider cast product of a dilated duct. It is seen in chronic renal failure.
In nephrotic syndrome many additional types of casts include broad and waxy casts if the condition is chronic (this is referred to as a telescopic urine with the presence of many casts).[3]
Formed by the breakdown of lipid-rich epithelial cells, these are hyaline casts with fat globule inclusions, yellowish-tan in color. If cholesterol or cholesterol esters are present, they are associated with the “Maltese cross” sign under polarized light. They are pathognomonic for high urinary protein nephrotic syndrome.
Formed by the adhesion of metabolic breakdown products or drug pigments, these casts are so named due to their discoloration. Pigments include those produced endogenously, such as hemoglobin in hemolytic anemia, myoglobin in rhabdomyolysis, and bilirubin in liver disease. Drug pigments, such as phenazopyridine, may also cause cast discoloration.
Though crystallized urinary solutes, such as oxalates, urates, or sulfonamides, may become enmeshed within a ketanaline cast during its formation, the clinical significance of this occurrence is not felt to be great.
The presence of red blood cells within the cast is always pathological, and is strongly indicative of glomerular damage, which can occur in glomerulonephritis from various causes or vasculitis, including granulomatosis with polyangiitis, systemic lupus erythematosus, post-streptococcal glomerulonephritis or Goodpasture’s syndrome. They can also be associated with renal infarction and subacute bacterial endocarditis. They are a yellowish-brown color and are generally cylindrical with sometimes ragged edges; their fragility makes inspection of a fresh sample necessary. They are usually associated with nephrotic syndromes or urinary tract injury.
Indicative of inflammation or infection, the presence of white blood cells within or upon casts strongly suggests pyelonephritis, a direct infection of the kidney. They may also be seen in inflammatory states, such as acute allergic interstitial nephritis, nephrotic syndrome, or post-streptococcal acute glomerulonephritis. White cells sometimes can be difficult to discern from epithelial cells and may require special staining. Differentiation from simple clumps of white cells can be made by the presence of hyaline matrix.
Given their appearance in pyelonephritis, these should be seen in association with loose bacteria, white blood cells, and white blood cell casts. Their discovery is likely rare, due to the infection-fighting efficiency of neutrophils, and the possibility of misidentification as a fine granular cast.
This cast is formed by inclusion or adhesion of desquamated epithelial cells of the tubule lining. Cells can adhere in random order or in sheets and are distinguished by large, round nuclei and a lower amount of cytoplasm. These can be seen in acute tubular necrosis and toxic ingestion, such as from mercury, diethylene glycol, or salicylate. In each case, clumps or sheets of cells may slough off simultaneously, depending of the focality of injury. Cytomegalovirus and viral hepatitis are organisms that can cause epithelial cell death as well.
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| リンク元 | 「尿沈渣」 |
| 関連記事 | 「sediment」「urinary」 |
| 赤血球 | ≧5個/HPF |
| 白血球 | ≧5個/HPF |
| 上皮細胞(正常) | 扁平上皮細胞をのぞく全て(移行上皮、尿細管上皮、円柱上皮) |
| 上皮細胞(異常) | すべて(卵円系脂肪体、多核巨細胞、封入体細胞) |
| 異型細胞 | 癌細胞 |
| 大食細胞 | ≧1個/HPF |
| 円柱 | ＜1個/HPFの硝子円柱をのぞく全て |
| 粘液系 | ≧1+ |
| 結晶 | 病的結晶(シスチン、チロシン、ロイシン、ビリルビン、コレステロール、DHA結晶)。正常結晶(尿酸結晶)で≧2+の時 |
| 細菌 | ≧1+(＞/HPFの桿菌) |
| 真菌 | すべて |
| 原虫 | すべて |
| 寄生虫 | すべて |
| 尿沈渣成分の基準値 | |
| 強拡大視野あたり(/HPF) | |
| 赤血球数 | 1/4-7≧ |
| 白血球数 | 1-2/4-7≧ |
| 上皮細胞数 | 1/10≧ |
| 円柱 | 1/20≧ |
| 液性 | 成分 | 形態 | 色 |
| 酸性 | 尿酸 | 菱形 | 黄褐色 |
| アルカリ性～酸性 | シュウ酸カルシウム | 正八面体 | |
| リン酸カルシウム | 板状、針状 | 灰白色 | |
| アルカリ性 | 炭酸カルシウム | 顆粒状ダンベル型 | 無色～灰白色 |
| リン酸アンモニウムマグネシウム | 長方形 | 無色 | |
| 尿酸アンモニウム | 棘のある小円状 | 黄褐色～茶褐色 | |
| 液性 | 病的結晶成分 | 形態 | 色 | 疾患 |
| シスチン | 正六角形板状構造 | 無色 | シスチン尿症 | |
| ロイシン | 円形放射状 | 重症肝障害 | ||
| チロシン | 針状 | |||
| ビリルビン | 針状 | |||
| コレステロール | 長方形板状 | 無色 | ネフローゼ症候群 |
| 液性 | 病的結晶成分 | 形態 | 色 | 疾患 |
| 尿酸 | 腫瘍崩壊症候群 | |||
| シュウ酸カルシウム | エチレングリコール中毒 |
| 上皮円柱 | 剥離した尿細管上皮細胞 | 尿細管の病変と尿細管腔の閉塞 | ネフローゼ症候群、急性尿細管壊死、アミロイドーシス、子癇、移植腎の急性拒絶反応 | |
| 顆粒円柱 | 崩壊した上皮円柱中の尿細管上皮細胞 | 急性腎盂腎炎、尿細管間質性腎炎、糸球体腎炎 | ||
| ろう様円柱 | 微細顆粒円柱が変性・脱水し均一無構造化 | 長期間の尿細管腔の局所的閉塞と無尿 | 慢性腎不全 | |
| 血球円柱 | 赤血球円柱 | 赤血球が尿細管腔内で集結 | 糸球体の出血 | 糸球体腎炎(IgA腎症、膜性増殖性腎炎、巣状糸球体硬化症、溶連菌感染後急性糸球体腎炎、ループス腎炎など)、血管炎、腎梗塞 |
| 白血球円柱 | 尿細管腔ないへの白血球の浸潤 | 急性腎盂腎炎、尿細管間質性腎炎、糸球体腎炎(溶連菌感染後急性糸球体腎炎、膜性増殖性腎炎、ループス腎炎、ANCA関連腎炎など) | ||
| 脂肪円柱 | 脂肪顆粒 | 重症ネフローゼ症候群、ループス腎炎、糖尿病腎症 | ||