Pal Jitendra Nath, Kar Maitreyee, Hazra Sunit, Basu Anindya
Department of Orthopaedics, Murshidabad Medical College, Station Road, Berhampore, District - Murshidabad, Pin - 742101. India.
Department of Anatomy, North Bengal Medical College, Sushrutnagar, District - Darjeeling. India.
J Orthop Case Rep. 2015 Oct-Dec;5(4):3-6. doi: 10.13107/jocr.2250-0685.331.
Solitary exostosis is common at the metaphysis of long bones, and rarely may it develop in the lower pole of the patella. Usually it stops growing after skeletal maturity unless complicated. When the growth continues after skeletal maturity, other rare possibilities need to be considered such as bizarre parosteal osteochondromatous proliferation (BPOP). Though solitary exostosis is common at the metaphysis of long bones, very rarely it also develops in lower pole of the patella. Usually they stop growing after skeletal maturity unless complicated. When it starts after skeletal maturity and continues to grow, other rare possibilities like bizarre parostealosteochondromatousproliferation (BPOP) are to be thought of.
21 years male student presented with anterior midline painless progressive swelling over right knee joint of one year duration which was hard, non-tender, fixed to patella but mobile with patella. X ray showed midline heterogeneously radio-opaque swelling attached to inferolateral aspect of the anterior surface of patella. Patellar out line is fully maintained except the narrow site of tumour attachment. After exposing through midline incision, the swelling was found to incorporate the patellar tendon completely and an anterior vertical midline cleavage was found. The mass was deliberately detached along the cleavage and from intact patellar tendon. Almost full range of knee movement is obtained in operation table. Immediate post operative 10° quadriceps lag was corrected with quadriceps setting exercises in two weeks time. Histopathological examination demonstrated thin layer of cartilage cover, irregular lamellar bone in deeper zone and spindle cells between them without cytoplasmic atypia. Plenty of cartilage cells in different stages of maturation are seen without column formation. Marrow elements are absent. Periosteum could not be demonstrated and there was no other evidence of malignancy. Features simulate 'bizarre parosteal osteochondromatous proliferation'. There is no recurrence in five years of follow up.
When exostosis like lesions arise from unusual site and at an unusual age group, other rare conditions need to be investigated. Though the final diagnosis of BPOP is obtained after careful histo-pathological examination, the clinico-radiological findings are also relevant. As literature search indicates, this is possibly second incidence where BPOP arised from sesamoid bone and first from patella.
孤立性骨软骨瘤常见于长骨的干骺端,很少发生于髌骨下极。通常在骨骼成熟后停止生长,除非出现并发症。当骨骼成熟后仍继续生长时,需要考虑其他罕见情况,如怪异的骨旁骨软骨瘤样增殖(BPOP)。尽管孤立性骨软骨瘤常见于长骨的干骺端,但也极少发生于髌骨下极。通常它们在骨骼成熟后停止生长,除非出现并发症。当在骨骼成熟后开始并持续生长时,需要考虑其他罕见情况,如怪异的骨旁骨软骨瘤样增殖(BPOP)。
一名21岁男性学生,右膝关节前正中线处出现无痛性进行性肿胀,持续一年,质地坚硬,无压痛,与髌骨相连但随髌骨活动。X线显示髌骨前表面下外侧附着有中线不均匀的不透射线肿胀。除肿瘤附着的狭窄部位外,髌骨轮廓完全保留。经中线切口暴露后,发现肿胀完全累及髌腱,并发现一条前垂直中线裂隙。肿块沿裂隙并从完整的髌腱上小心分离。在手术台上几乎获得了膝关节的全范围活动。术后立即出现的10°股四头肌滞后在两周内通过股四头肌锻炼得到纠正。组织病理学检查显示有一层薄的软骨覆盖,深部区域有不规则的板层骨,其间有梭形细胞,无细胞质异型性。可见大量处于不同成熟阶段的软骨细胞,无柱状形成。无骨髓成分。未发现骨膜,也无其他恶性证据。其特征类似“怪异的骨旁骨软骨瘤样增殖”。随访五年无复发。
当骨软骨瘤样病变出现在不寻常的部位和不寻常的年龄组时,需要调查其他罕见情况。尽管BPOP的最终诊断是在仔细的组织病理学检查后得出的,但临床放射学表现也很重要。正如文献检索所示,这可能是BPOP起源于籽骨的第二例,也是首例起源于髌骨的病例。