炎症Inflammation · 口腔黏膜 · 消化系统 · NTP ntp-0224
诊断要点:炎症无论何时出现,均应予以诊断、分级,并给出一个修饰词以指明炎症的持续时间或类型(即 急性(acute)、化脓性(suppurative)、慢性(chronic)、慢性 active 或 肉芽肿性(granulomatous))。
病变描述
口腔内的炎症通常继发于异物或灌胃操作造成的创伤性损伤,或继发于化学物质引起的坏死。病变内可能可见感染性病原体,通常为细菌和真菌等机会性微生物(Figure 1、Figure 2)。在NTP研究中,炎症有五个标准类别:急性(急性(acute))、化脓性(化脓性(suppurative))(Figure 1、Figure 2)、慢性(慢性(chronic))、慢性活动性(慢性 active)(Figure 3、Figure 4)和肉芽肿性(肉芽肿性(granulomatous))。在急性炎症(急性 inflammation)中,主要浸润细胞为中性粒细胞(neutrophil),但也可能存在较少的巨噬细胞和淋巴细胞。还可能有水肿或充血的表现。中性粒细胞也是化脓性炎症(化脓性 inflammation)中的主要浸润细胞类型,但中性粒细胞聚集,且其中许多已变性(化脓性渗出物)。渗出物中还可能存在细胞碎片(来自 resident 细胞群和浸润白细胞)、含纤维蛋白的蛋白性液体、较少的巨噬细胞、偶见的淋巴细胞或浆细胞,以及可能的感染性病原体。肉眼观察,这些病变的特征为脓液的存在。渗出物周围的组织可能含有成纤维细胞、纤维结缔组织和混合性炎症细胞,具体取决于病变的慢性程度。慢性炎症(慢性 inflammation)中以淋巴细胞为主。慢性活动性炎症(慢性 active inflammation)中也以淋巴细胞为主,但也存在显著数量的中性粒细胞。两种病变均可能含有巨噬细胞。肉芽肿性炎症(肉芽肿性 inflammation)是慢性炎症的另一种形式,但该诊断要求存在显著数量的聚集性、大型、活化巨噬细胞、上皮样巨噬细胞或多核巨细胞。
诊断与分级建议(NTP 共识)
炎症无论何时出现,均应予以诊断、分级,并给出一个修饰词以指明炎症的持续时间或类型(即 急性(acute)、化脓性(suppurative)、慢性(chronic)、慢性 active 或 肉芽肿性(granulomatous))。严重程度分级取决于受累区域的范围和细胞浸润的密度。符合脓肿的病变诊断为化脓性炎症。继发于其他病变(如溃疡、糜烂或坏死)的炎症不应单独诊断,除非严重程度足以支持单独诊断。然而,如果炎症被认为是原发病变并且是相关病变(溃疡、糜烂、坏死等)的原因,则应诊断炎症并在叙述中描述继发病变。细菌、真菌或其他机会性微生物不单独诊断。病变内的异物仅在被认为是原发病变(即炎症的原因)时才应诊断。如果病理学家认为异物是在炎症之后引入的,则应在病理学叙述中描述异物,但不单独诊断。
图谱


英文原文
展开 NTP 官方英文描述与建议
Comment:
Inflammation in the oral cavity is often secondary to traumatic injury from foreign bodies or gavage procedure or to necrosis from chemical agents. Infectious agents, usually opportunistic organisms such as bacteria and fungi, may be seen within the lesion ( Figure 1 and Figure 2 ). In NTP studies, there are five standard categories of inflammation: acute, suppurative ( Figure 1 and Figure 2 ), chronic, chronic active ( Figure 3 and Figure 4 ), and granulomatous. In acute inflammation , the predominant infiltrating cell is the neutrophil, though fewer macrophages and lymphocytes may also be present. There may also be evidence of edema or hyperemia. The neutrophil is also the predominant infiltrating cell type in suppurative inflammation , but the neutrophils are aggregated, and many of them are degenerate (suppurative exudate). Cell debris, both from the resident cell populations and from infiltrating leukocytes; proteinaceous fluid containing fibrin; fewer macrophages; occasional lymphocytes or plasma cells; and, possibly, an infectious agent may also be present in within the exudate. Grossly, these lesions would be characterized by the presence of pus. The tissue surrounding the exudate may contain fibroblasts, fibrous connective tissue, and mixed inflammatory cells, depending on the chronicity of the lesion. Lymphocytes predominate in chronic inflammation . Lymphocytes also predominate in chronic active inflammation , but there are also a significant number of neutrophils. Both lesions may contain macrophages. Granulomatous inflammation is another form of chronic inflammation, but this diagnosis requires the presence of a significant number of aggregated, large, activated macrophages, epithelioid macrophages, or multinucleated giant cells.
Recommendation:
Whenever present, inflammation should be diagnosed, graded, and given a modifier that indicates the duration or type of inflammation (i.e., acute, suppurative, chronic, chronic active, or granulomatous). The severity grade depends on the extent of the area affected and the density of the cellular infiltrate. Lesions consistent with an abscess are diagnosed as suppurative inflammation. Inflammation that is secondary to another lesion, such as ulcer, erosion, or necrosis, should not be diagnosed separately unless warranted by severity. If, however, the inflammation is considered the primary lesion and is the cause of the associated lesions (ulcer, erosion, necrosis, etc.), then the inflammation should be diagnosed and the secondary lesions described in the narrative. Bacteria, fungi, or other opportunistic organisms are not diagnosed separately. Foreign material within the lesion should be diagnosed only if it considered the primary lesion (i.e., the cause of the inflammation). If the pathologist feels the foreign material was introduced subsequent to the inflammation, then the foreign material should be described in the pathology narrative but not diagnosed separately.
来源与引用
原始条目:https://ntp.niehs.nih.gov/atlas/nnl/alimentary-system/oral-mucosa/Inflammation
图谱总目录:NTP Nonneoplastic Lesion Atlas。 内容属美国联邦政府作品(公有领域),可引用;引用时请标注来源。
建议引用格式:NTP Nonneoplastic Lesion Atlas. Inflammation (oral-mucosa). LabSmart 中文版:
https://www.labsmart.cn/ntp/oral-mucosa-inflammation.html
中文图谱总页(可展开对照全部 595 条):https://www.labsmart.cn/ntp-atlas.html#oral-mucosa-inflammation