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Psammomatoid Juvenile Ossifying Fibroma of the Mandible – A Histochemical insight!

机译:下颌骨类软骨样骨化性纤维瘤–组织化学见解!

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Juvenile ossifying fibroma (JOF) are fibro osseous lesions that mostly occur in children. Although a benign entity, JOF is known to be locally aggressive and has a high tendency to reoccur. Two distinctive microscopic patterns have been described; a trabecular variant and a Psammomatoid variant. This latter variant is predominantly a craniofacial lesion and occurs rarely in the jaws. We report a rare case of Psammomatoid Juvenile Ossifying that occurred in the mandible of a young boy along with review of the relevant literature. In addition, the pathology of the lesion was also analyzed with picrosirus red stain and polarizing microscopy Introduction Juvenile Ossifying fibroma is a fibro-osseous entity that arises within the craniofacial bones of young individuals below 15 years of age [1] . Juvenile Ossifying fibroma is a broad term to describe two distinct histopathological variants: Trabacular Juvenile Ossifying fibroma which is distinguished by the presence of trabaculae of fibrillar osteoid and woven bone and Psammomatoid Juvenile Ossifying fibroma (PsJOF) that is characterised by the presence of small uniform spherical ossicles that resemble Psammoma bodies [2] . PsJOF was first reported by Benjamins in 1938, who called the lesion “osteoid fibroma with atypical ossification of the frontal sinus” [3] . Later, Gogl in 1949 reported two cases of what he called “Psammomatoid ossifying fibroma of the nose and paranasal sinus” [4] . In 1952, Johnson termed the same lesion “Juvenile active ossifying fibroma” and described it as a cellular mass which generates innumerable small uniform sized osteoid bodies [5] . Makek in his review of fibroosseous lesions categorized these lesions as Psammous desmo-osteoblastomas [6] . Although PsJOF is an aggressive lesion with a predilection for children in the age range of 5-15 years [7] there are reports where the patient age ranged from 3 months to 72 years [568] A slight male predominance has been observed in several case reports and clinico-pathological studies of PsJOF [2689].Samik El Mofty [2] observed a significant demographic difference between the two variants of Juvenile Ossifying fibroma, while the trabecular variant is predominantly a gnathic lesion, with a predilection for the maxilla, PsJOF occurs overwhelmingly in the sinonasal and orbital bones. Johnson et al [5] and Makek [6] in their case series reports also found that 70% of the PsJoF’s occurred in the Paranasal sinus, 20% in the maxilla and only about 10% in the mandible. Here, we report an additional case of PsJOF that occurred in the mandible an uncommon site for this PsJOF. The histopathology of the lesion was also analysed with the aid of picrosirus red stain and polarizing microscopy to correlate the pathology of the lesion with its clinical behaviour. Case report A 13 year old boy reported to dental clinic of Manipal college of Dental sciences, Manipal in June 2006 with a chief complaint of a swelling on the right side of his face.. The swelling had developed 2 months back, and the size and firmness of the swelling had remained the same since then. An extra Oral examination revealed a 4x 4 cm swelling on the right body of the mandible extending from the angle of the mouth to the inferior body of the mandible (Fig1). The swelling was bony hard in consistency. There was no discharge pus, parasthesia of the lip or restricted mouth opening.
机译:少年骨化性纤维瘤(JOF)是多发于儿童的纤维性骨病变。尽管JOF是一个良性实体,但它在当地具有侵略性,而且发生的可能性很高。已经描述了两种不同的微观模式。小梁变异体和类滑膜变体。后一种变体主要是颅面病变,很少发生在颌骨中。我们报告了一个小男孩下颌骨发生的类囊性少年骨化症,并回顾了相关文献。此外,还用picirirusus红色染色和偏光显微镜对病变的病理学进行了分析。简介少年骨化性纤维瘤是一种纤维骨实体,出现在15岁以下的年轻人的颅面骨内[1]。幼年骨化性纤维瘤是一个广义术语,用于描述两种不同的组织病理学变异:小梁性骨化性纤维瘤,其特征是存在成纤维状骨样瘤和编织骨的小梁,以及Psammomatoid幼化骨化性纤维瘤(PsJOF),其特征是存在小的均匀球形球形类似于沙门氏菌体的小骨[2]。本杰明斯于1938年首次报道了PsJOF,他称病变为“具有额窦非典型骨化的骨样纤维瘤” [3]。后来,Gogl在1949年报告了两例他所说的“鼻窦和鼻旁窦的类滑膜骨化性纤维瘤” [4]。 1952年,约翰逊将同一病变称为“青少年活动性骨化性纤维瘤”,并将其描述为细胞团,可产生无数小的均匀大小的类骨质体[5]。马克(Markk)在他对纤维性病变的评论中将这些病变归类为滑脱性成骨成骨细胞瘤[6]。尽管PsJOF是一种侵袭性病变,偏爱5-15岁的儿童[7],但有报道称患者年龄在3个月至72岁之间[568]在一些情况下,男性占主导地位PsJOF [2689]的报道和临床病理研究。SamikEl Mofty [2]观察到两个青少年骨化性纤维瘤变体之间存在显着的人口统计学差异,而小梁变体主要是棘突性病变,上颌骨偏向于PsJOF。绝大多数发生在鼻窦和眶骨中。 Johnson等[5]和Makek [6]在他们的病例系列报告中还发现,PsJoF的70%发生在副鼻窦,上颌的20%和下颌骨的约10%。在这里,我们报告了另一例PsJOF,该病例发生在该PsJOF的下颌骨的罕见部位。还借助皮克西鲁斯红染色和偏光显微镜分析了病变的组织病理学,以将病变的病理学与其临床行为相关联。病例报告2006年6月,一个13岁的男孩向马尼帕尔市马尼帕尔牙科科学学院的牙科诊所报告,主要抱怨面部右侧肿胀。肿胀在2个月后出现,大小和从那时起,肿胀的坚硬程度一直保持不变。额外的口腔检查发现,在下颌骨的右身体上有4x 4 cm的肿胀,从嘴角延伸到下颌骨的下体(图1)。肿胀很难保持一致。没有脓液,嘴唇感觉异常或张口受限。

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