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Corrective osteotomy for cubitus varus using the Image Fusion System 利用图像融合系统对拇趾外翻进行矫正截骨术
Pub Date : 2024-09-01 Epub Date: 2024-03-08 DOI: 10.1016/j.joscr.2024.02.001
Junichiro Morita , Yuichi Yoshii , Takushi Nakatani , Takeshi Ogawa , Hajime Mishima , Tomoo Ishii

Background

An Image Fusion System was developed and clinically applied to project preoperative planning images onto intraoperative fluoroscopic images. We herein report a case of corrective osteotomy for cubitus varus using the Image Fusion System.

Case presentation

The present case is a 34-year-old female with cubitus varus. The patient had a varus elbow deformity and elbow pain due to the malunion of a distal humerus fracture in childhood. We performed corrective osteotomy under general anesthesia using the Image Fusion System.

Bone union was achieved approximately 3 months after surgery. The Mayo elbow performance score increased from 60 before surgery to 100 after surgery. The postoperative carrying angle of the elbow joint increased from −17° before surgery to 7° after surgery.

Conclusion

The Image Fusion System may be one of the methods used to assist corrective osteotomy for cubitus varus.

背景图像融合系统被开发出来并应用于临床,将术前规划图像投射到术中透视图像上。本病例是一名 34 岁的女性,患有肘关节立方体外翻。患者在童年时曾因肱骨远端骨折而导致肘关节屈曲畸形和肘关节疼痛。我们在全身麻醉下使用图像融合系统进行了矫正截骨术。梅奥肘关节功能评分从术前的 60 分升至术后的 100 分。术后肘关节的承载角度从术前的-17°增加到术后的7°。
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引用次数: 0
Chronic Achilles tendon sleeve avulsion treated by combination of V–Y tendon plasty and suture bridge technique: A case report 结合 V-Y 肌腱成形术和缝合桥接技术治疗慢性跟腱套撕脱:病例报告
Pub Date : 2024-09-01 Epub Date: 2024-04-01 DOI: 10.1016/j.joscr.2024.03.003

Background

In the cases of Achilles tendon sleeve avulsion with a larger tendon defect, the surgeon should be prepared to perform reconstruction of the tendon insertion as well as the tendon defect. This report details a case of a chronic Achilles tendon sleeve avulsion in a 52-year-old female who was successfully treated with a combination of V–Y tendon plasty and suture bridge technique.

Case presentation

A 52-year-old female presented to our hospital with a 3-month history of persistent posterior ankle pain. Based on physical examination and image findings, the patient was diagnosed with chronic Achilles tendon sleeve avulsion and treated operatively. Because of a large tendon defect, a combination of V–Y tendon plasty and suture bridge technique was performed. At 2 years postoperatively, the patient had no symptoms or functional impairment.

Conclusions

Although a long-term follow-up is required in this case, this operative procedure yielded good short-term results.

背景在跟腱套撕脱并伴有较大肌腱缺损的病例中,外科医生应做好重建肌腱插入部和肌腱缺损的准备。本报告详细介绍了一例慢性跟腱套撕脱的病例,患者为 52 岁女性,采用 V-Y 肌腱成形术和缝合桥接技术成功治疗。根据体格检查和影像学检查结果,患者被诊断为慢性跟腱套撕脱,并接受了手术治疗。由于肌腱缺损面积较大,因此采用了 V-Y 肌腱成形术和缝合桥接技术。结论虽然该病例需要长期随访,但这种手术方法取得了良好的短期效果。
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引用次数: 0
Long-term outcomes of BCG osteomyelitis in infants: Epiphyseal regeneration and minimal leg-length discrepancy after 10 years 卡介苗骨髓炎对婴儿的长期影响:骺板再生和 10 年后最小腿长差异
Pub Date : 2024-07-01 Epub Date: 2024-02-01 DOI: 10.1016/j.joscr.2024.01.003
Satomi Abe, Yusuke Sasaki, Keisuke Matsukura, Hiroshi Ito

Background

Bacillus Calmette-Guérin (BCG) is a vaccine to prevent tuberculosis. Complications in infants and children include BCG osteitis and osteomyelitis of the metaphysis or epiphysis of long bones. There have been few reports of long-term follow-up. We investigated 10-year outcomes based on X-rays and physical examinations.

Case presentation

We described two individuals who developed BCG osteomyelitis after vaccination (Tokyo 172 strain) at 3 months old. Both cases underwent a biopsy of the infected epiphyseal lesion, irrigation from the metaphysis through the center of the growth plates, and received two anti-tuberculosis drugs: rifampicin and isoniazid. At the 10-year follow-up, the affected epiphysis had regenerated and both cases showed a leg-length discrepancy of less than 1 cm due to overgrowth.

Conclusions

This study reported on the long-term outcomes of two cases of BCG epiphyseal osteomyelitis in infants, revealing favorable results with regenerated epiphysis and minimal leg-length discrepancy.

背景卡介苗(BCG)是一种预防结核病的疫苗。婴儿和儿童的并发症包括卡介苗骨炎和长骨干骺端或骨骺端的骨髓炎。有关长期随访的报道很少。我们根据 X 光片和体格检查结果对 10 年的治疗效果进行了调查。病例介绍我们描述了两个在 3 个月大时接种卡介苗(东京 172 株)后出现卡介苗骨髓炎的病例。两个病例都接受了骺端感染病灶的活检,从干骺端通过生长板中心进行灌洗,并接受了两种抗结核药物治疗:利福平和异烟肼。结论 本研究报告了两例卡介苗骺端骨髓炎婴儿的长期疗效,结果显示,两例病例均取得了良好的疗效,骨骺再生,腿长差异极小。
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引用次数: 0
Iatrogenic spinal subarachnoid hematoma and cauda equina compression after preoperative myelography for lumbar revision surgery: A case report 腰椎翻修手术术前髓鞘造影术后先天性脊柱蛛网膜下腔血肿和马尾受压:病例报告
Pub Date : 2024-07-01 Epub Date: 2024-01-09 DOI: 10.1016/j.joscr.2023.12.006
Naoki Okamoto, Rentaro Okazaki, Seiichi Azuma

Background

Lumbar puncture for myelography can cause incidental vascular injury, but rarely results in spinal hematoma formation.

Case presentation

A 73-year-old man without coagulopathy underwent preoperative myelography for lumbar revision. Magnetic resonance imaging revealed L2/3 and L4/5 canal stenoses. A subsequent atraumatic lumbar puncture was performed in the previously decompressed L3/4 interlaminar space. After the procedure, the patient presented with gradually worsening neurological disorder. Emergency magnetic resonance imaging revealed localized subarachnoid hematoma at the L3-4 level. The neurological disorder improved remarkably after L2-L5 laminectomy and hematoma removal.

Conclusions

During preoperative myelography for lumbar revision, lumbar puncture of a previously decompressed segment should be avoided if canal stenotic lesions exist in both craniocaudal adjacent segments. Incidental vascular injury and impaired cerebrospinal fluid flow due to adjacent canal stenoses may cancel the washout process of hemorrhage and cause subarachnoid hematoma.

背景腰椎穿刺进行脊髓造影可能会造成意外的血管损伤,但很少会导致脊髓血肿的形成。病例介绍一名 73 岁的男性因腰椎翻修而接受了术前脊髓造影,但他没有凝血功能障碍。磁共振成像显示 L2/3 和 L4/5 椎管狭窄。随后在先前减压的 L3/4 椎间隙进行了无创腰椎穿刺。术后,患者的神经功能紊乱逐渐加重。急诊磁共振成像显示,L3-4 水平有局部蛛网膜下血肿。结论在腰椎翻修的术前脊髓造影中,如果两个颅尾相邻节段都存在椎管狭窄病变,则应避免对先前减压的节段进行腰椎穿刺。相邻管腔狭窄造成的意外血管损伤和脑脊液流动障碍可能会取消出血的冲洗过程并导致蛛网膜下血肿。
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引用次数: 0
Metastatic malignant glomus tumor resistant to pazopanib, a multikinase inhibitor: A case report and review of literature 对多激酶抑制剂帕唑帕尼耐药的转移性恶性胶状体瘤:病例报告和文献综述
Pub Date : 2024-07-01 Epub Date: 2024-01-12 DOI: 10.1016/j.joscr.2024.01.001
Kengo Kawaguchi , Makoto Endo , Suguru Fukushima , Takeshi Hirose , Akira Nabeshima , Toshifumi Fujiwara , Yoshinao Oda , Yasuharu Nakashima

Background

Malignant glomus tumors are extremely rare soft tissue tumors that are rich in tumor vessels. Due to its rarity, no treatment strategy other than resection has been established. Pazopanib, a multikinase inhibitor, is expected to improve the prognosis of patients with soft tissue sarcoma. However, there are no reports on the clinical outcomes of pazopanib in patients with malignant glomus tumors.

Case presentation

A 74-year-old man with a history of neurofibromatosis type 1 was diagnosed with a malignant glomus tumor on his left thigh, with multiple lung metastases at initial presentation. Doxorubicin was administered followed by pazopanib; however, tumor progression was not arrested.

Conclusion

To the best of our knowledge, this is the first reported case of a malignant glomus tumor treated with pazopanib. Further investigations on chemotherapy in patients with malignant glomus tumors are needed.

背景 恶性龟头瘤是一种极为罕见的软组织肿瘤,肿瘤血管丰富。由于其罕见性,除切除术外,尚无其他治疗策略。帕唑帕尼是一种多激酶抑制剂,有望改善软组织肉瘤患者的预后。病例介绍 一位 74 岁的男性被诊断为左大腿恶性胶质瘤,初诊时有多处肺转移。据我们所知,这是首例用帕唑帕尼治疗恶性肉芽肿的病例。据我们所知,这是用帕唑帕尼治疗恶性胶状体瘤的首例报道,还需要对恶性胶状体瘤患者的化疗进行进一步研究。
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引用次数: 0
Compartment syndrome of the foot with Lisfranc fracture dislocation treated by a 2-incision approach: A case report 采用双切口方法治疗伴有Lisfranc骨折脱位的足部室间隔综合征:病例报告
Pub Date : 2024-07-01 Epub Date: 2024-01-26 DOI: 10.1016/j.joscr.2024.01.004
Hozumi Kumano , Keisoh Tsuboi , Tomohiko Murakami , Kazuki Yonei , Hiroshi Murao

Background

Compartment syndrome of the foot(CSF)can be triggered by Lisfranc fracture dislocations. CSF has been generally treated using a 3-incision approach. We report a case in which CSF with Lisfranc fracture dislocation was treated by a 2-incision approach.

Case presentation

A 50-year-old man who suffered from a motorcycle accident was presented at our hospital. The patient had severe pain and swelling of his foot. A Lisfranc fracture dislocation was observed, and intracompartmental pressure showed 104 mmHg in the medial compartment. We diagnosed CSF with Lisfranc fracture dislocation. Decompression of all compartments of the foot and open reduction and fixation were performed using a 2-incision approach. Six months after surgery, the patient returned to work. The Japanese Society for Surgery of the Foot midfoot scale score was 74 points 13 months after surgery.

Conclusions

The 2-incision approach is useful for CSF associated with Lisfranc fracture dislocations.

背景足部椎间隙综合征(CSF)可由Lisfranc骨折脱位引发。CSF一般采用3切口方法治疗。我们报告了一例采用两切口方法治疗 CSF 并伴有 Lisfranc 骨折脱位的病例。患者足部剧烈疼痛和肿胀。我们观察到患者有一处 Lisfranc 骨折脱位,内侧间室压力显示为 104 mmHg。我们诊断其为 CSF Lisfranc 骨折脱位。我们采用双切口方法对患者的足部各关节间隙进行了减压,并进行了切开复位和固定术。术后六个月,患者重返工作岗位。结论:两切口方法适用于与Lisfranc骨折脱位相关的CSF。
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引用次数: 0
Masquelet technique for reconstruction of a large osteomyelitis defect following open fracture of the radius: A pediatric case report 用 Masquelet 技术重建桡骨开放性骨折后的大面积骨髓炎缺损:儿科病例报告
Pub Date : 2024-07-01 Epub Date: 2024-01-24 DOI: 10.1016/j.joscr.2024.01.006
Koh Terauchi , Yohei Shimada , Yosuke Kano , Shu Somemura , Takeshi Arai , Kenichi Murakami , Jun Kakizaki , Hisateru Niki

Background

We report a case of a child who underwent the Masquelet technique for the reconstruction of bone defects caused by osteomyelitis of the radius.

Case presentation

A 9-year-old girl fell off playground equipment and sustained an open fracture of the forearm. She underwent emergency debridement and K-wire fixation. Swelling and redness of the forearms developed 1 month after the injury. Simple radiography revealed bone destruction of the radius, and osteomyelitis was diagnosed. Debridement was performed, and 6.5 cm of the radius was resected. After 8 weeks of treatment with antibiotics effective against the causative agent Enterobacter cloacae, the bone defect was reconstructed using the Masquelet technique. Bone fusion was achieved 3 months postoperatively, with no recurrence of infection during a 4-year follow-up.

Conclusions

The Masquelet technique could be an effective treatment option for upper-extremity bone defects in children.

背景我们报告了一例采用 Masquelet 技术重建桡骨骨髓炎引起的骨缺损的儿童病例。病例介绍一名 9 岁女孩从游乐设施上摔下,造成前臂开放性骨折。她接受了紧急清创和 K 线固定。受伤 1 个月后,前臂出现肿胀和发红。简单的放射线检查显示桡骨骨质破坏,诊断为骨髓炎。进行了清创术,切除了 6.5 厘米长的桡骨。使用对致病菌丁香肠杆菌有效的抗生素治疗 8 周后,采用马斯奎莱技术重建了骨缺损。结论 Masquelet 技术是治疗儿童上肢骨缺损的有效方法。
{"title":"Masquelet technique for reconstruction of a large osteomyelitis defect following open fracture of the radius: A pediatric case report","authors":"Koh Terauchi ,&nbsp;Yohei Shimada ,&nbsp;Yosuke Kano ,&nbsp;Shu Somemura ,&nbsp;Takeshi Arai ,&nbsp;Kenichi Murakami ,&nbsp;Jun Kakizaki ,&nbsp;Hisateru Niki","doi":"10.1016/j.joscr.2024.01.006","DOIUrl":"10.1016/j.joscr.2024.01.006","url":null,"abstract":"<div><h3>Background</h3><p>We report a case of a child who underwent the Masquelet technique for the reconstruction of bone defects caused by osteomyelitis of the radius.</p></div><div><h3>Case presentation</h3><p>A 9-year-old girl fell off playground equipment and sustained an open fracture of the forearm. She underwent emergency debridement and K-wire fixation. Swelling and redness of the forearms developed 1 month after the injury. Simple radiography revealed bone destruction of the radius, and osteomyelitis was diagnosed. Debridement was performed, and 6.5 cm of the radius was resected. After 8 weeks of treatment with antibiotics effective against the causative agent <em>Enterobacter cloacae</em>, the bone defect was reconstructed using the Masquelet technique. Bone fusion was achieved 3 months postoperatively, with no recurrence of infection during a 4-year follow-up.</p></div><div><h3>Conclusions</h3><p>The Masquelet technique could be an effective treatment option for upper-extremity bone defects in children.</p></div>","PeriodicalId":100743,"journal":{"name":"JOS Case Reports","volume":"3 2","pages":"Pages 127-130"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772964824000078/pdfft?md5=f3c2881a5375a2e3550b80be32dba0cf&pid=1-s2.0-S2772964824000078-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139638757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Paraneoplastic syndrome due to dedifferentiated liposarcoma producing granulocyte colony-stimulating factor and interleukin-6 产生粒细胞集落刺激因子和白细胞介素-6的分化型脂肪肉瘤导致的副肿瘤综合征
Pub Date : 2024-07-01 Epub Date: 2023-12-22 DOI: 10.1016/j.joscr.2023.12.001
Tomoya Matsunobu , Akira Maekawa , Masato Yoshimoto , Kosuke Makihara , Masanori Hisaoka , Yukihide Iwamoto

Background

Pyrexia and leukocytosis are rare symptoms of paraneoplastic syndrome in patients with solid tumors.

Case presentation

A 56-year-old man presented with a large mass in the left thigh, and intermittent high fevers and leukocytosis. Core-needle biopsy resulted in a pathological diagnosis of dedifferentiated liposarcoma. Laboratory test revealed that granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6) production levels were significantly elevated. Soon after surgical excision of the soft tissue sarcoma, the leukocytosis and systemic symptoms had dramatically resolved. After completing adjuvant chemotherapy, no tumor local recurrence or distant metastases have been found during 26 months of follow-up.

Conclusions

To the best of our knowledge, this is the second case report of a patient with dedifferentiated liposarcoma producing both G-CSF and IL-6. Clinicians should be aware that soft tissue sarcoma could cause pyrexia and leukocytosis as part of a paraneoplastic syndrome due to G-CSF and IL-6 production.

背景厌食和白细胞增多是实体瘤患者出现副肿瘤综合征的罕见症状。病例介绍一名 56 岁的男子因左大腿出现巨大肿块、间歇性高烧和白细胞增多而就诊。核心针活检的病理诊断为脂肪肉瘤。实验室检查显示,粒细胞集落刺激因子(G-CSF)和白细胞介素-6(IL-6)分泌水平明显升高。手术切除软组织肉瘤后不久,白细胞增多和全身症状明显缓解。据我们所知,这是第二例同时产生 G-CSF 和 IL-6 的脂肪肉瘤患者。临床医生应该意识到,软组织肉瘤可因产生 G-CSF 和 IL-6 而导致热病和白细胞增多,这是副瘤综合征的一部分。
{"title":"Paraneoplastic syndrome due to dedifferentiated liposarcoma producing granulocyte colony-stimulating factor and interleukin-6","authors":"Tomoya Matsunobu ,&nbsp;Akira Maekawa ,&nbsp;Masato Yoshimoto ,&nbsp;Kosuke Makihara ,&nbsp;Masanori Hisaoka ,&nbsp;Yukihide Iwamoto","doi":"10.1016/j.joscr.2023.12.001","DOIUrl":"10.1016/j.joscr.2023.12.001","url":null,"abstract":"<div><h3>Background</h3><p>Pyrexia and leukocytosis are rare symptoms of paraneoplastic syndrome in patients with solid tumors.</p></div><div><h3>Case presentation</h3><p>A 56-year-old man presented with a large mass in the left thigh, and intermittent high fevers and leukocytosis. Core-needle biopsy resulted in a pathological diagnosis of dedifferentiated liposarcoma. Laboratory test revealed that granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6) production levels were significantly elevated. Soon after surgical excision of the soft tissue sarcoma, the leukocytosis and systemic symptoms had dramatically resolved. After completing adjuvant chemotherapy, no tumor local recurrence or distant metastases have been found during 26 months of follow-up.</p></div><div><h3>Conclusions</h3><p>To the best of our knowledge, this is the second case report of a patient with dedifferentiated liposarcoma producing both G-CSF and IL-6. Clinicians should be aware that soft tissue sarcoma could cause pyrexia and leukocytosis as part of a paraneoplastic syndrome due to G-CSF and IL-6 production.</p></div>","PeriodicalId":100743,"journal":{"name":"JOS Case Reports","volume":"3 2","pages":"Pages 73-77"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S277296482300062X/pdfft?md5=4ee89d4e8c2ee30dcba438eb97f9e1c2&pid=1-s2.0-S277296482300062X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139022635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Essex-Lopresti injury treated with radial head replacement and interosseous membrane reconstruction using synthetic graft: A case report 使用合成移植物进行桡骨头置换和骨间膜重建术治疗埃塞克斯-洛普雷斯蒂损伤:病例报告
Pub Date : 2024-07-01 Epub Date: 2024-01-05 DOI: 10.1016/j.joscr.2023.12.004
Keisuke Koizumi, Hiroshi Yamazaki

Background

Essex-Lopresti injury (ELI) is a rare injury accompanied by radioulnar dissociation with radial head (RH) fracture, interosseous membrane (IOM) rupture, and distal radioulnar joint (DRUJ) disruption. The reconstruction of IOM for the acute ELI remains controversial and challenging.

Case presentation

We report an acute ELI successfully treated with RH replacement, triangular fibrocartilage complex (TFCC) repair, and IOM reconstruction using synthetic graft through the radial and ulnar bone tunnels, in a 59-year-old man. Seven years after the injury, he had no complaints of wrist pain. The radiographs revealed no evidence of hardware loosening or enlargement in the size of the bone tunnels, in spite of slight accelerated capitellar wear and osteoarthritic change in DRUJ.

Conclusion

This study presents an alternative treatment for acute ELI by the combination with RH replacement, TFCC repair and IOM reconstruction using a synthetic graft. Longitudinal forearm stability may have reduced load transfer to the RH prosthesis.

背景Essex-Lopresti损伤(ELI)是一种罕见的损伤,伴有桡骨头(RH)骨折、骨间膜(IOM)破裂和远端桡肘关节(DRUJ)破坏的桡肘关节离断。我们报告了一名 59 岁男性的急性桡侧腓骨离断术(ELI),该患者成功接受了桡骨头置换术、三角纤维软骨复合体(TFCC)修复术以及通过桡骨和尺骨隧道使用合成移植物重建桡侧腓骨离断术。受伤七年后,他再也没有抱怨过手腕疼痛。尽管髌骨磨损略有加速,DRUJ也出现了骨关节炎性改变,但X光片显示没有硬件松动或骨隧道扩大的迹象。前臂纵向的稳定性可能会减少向RH假体传递的负荷。
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引用次数: 0
Chronic proximal tibial aseptic osteitis diagnosed as SAPHO syndrome ameliorated with oral methotrexate: A case report 被诊断为 SAPHO 综合征的慢性胫骨近端无菌性骨炎在口服甲氨蝶呤后有所好转:病例报告
Pub Date : 2024-07-01 Epub Date: 2024-01-13 DOI: 10.1016/j.joscr.2024.01.002
Takuya Izumiyama , Yu Mori , Yasuaki Kuriyama , Ryuichi Kanabuchi , Naoko Mori , Toshimi Aizawa

Background

Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a multiple disease group affecting the bones and joints. However, treatment for severe SAPHO syndrome is sometimes difficult, and treatment strategies have not been constructed.

Case presentation

We experienced a 23-year-old male with isolated chronic aseptic osteitis of the right proximal tibia, which was detected with magnetic resonance imaging and bone scintigraphy. We administered oral nonsteroidal anti-inflammatory drugs and local steroid injection, but his symptoms were not improved. Next, we administered oral methotrexate, which caused improvement effects, including decreased swelling and knee pain. In addition, the contrasted osteitis lesion in the proximal tibia demonstrated by magnetic resonance imaging completely disappeared.

Conclusions

Reports of osteitis in SAPHO syndrome resolved by methotrexate were rare. Although the effect of methotrexate on SAPHO syndrome was controversial, methotrexate should be considered for patients with refractory SAPHO syndrome before biologics.

背景滑膜炎、痤疮、脓疱病、骨质增生和骨炎(SAPHO)综合征是一种影响骨骼和关节的多发性疾病。病例介绍我们接诊了一名 23 岁男性患者,他患有右胫骨近端孤立性慢性无菌性骨炎,经磁共振成像和骨闪烁成像检查发现了该病。我们为他口服了非甾体抗炎药,并进行了局部类固醇注射,但症状并未改善。随后,我们口服了甲氨蝶呤,效果有所改善,包括肿胀和膝关节疼痛减轻。此外,磁共振成像显示的胫骨近端对比骨炎病灶完全消失。尽管甲氨蝶呤对 SAPHO 综合征的疗效存在争议,但对于难治性 SAPHO 综合征患者,在使用生物制剂之前,应考虑使用甲氨蝶呤。
{"title":"Chronic proximal tibial aseptic osteitis diagnosed as SAPHO syndrome ameliorated with oral methotrexate: A case report","authors":"Takuya Izumiyama ,&nbsp;Yu Mori ,&nbsp;Yasuaki Kuriyama ,&nbsp;Ryuichi Kanabuchi ,&nbsp;Naoko Mori ,&nbsp;Toshimi Aizawa","doi":"10.1016/j.joscr.2024.01.002","DOIUrl":"10.1016/j.joscr.2024.01.002","url":null,"abstract":"<div><h3>Background</h3><p>Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a multiple disease group affecting the bones and joints. However, treatment for severe SAPHO syndrome is sometimes difficult, and treatment strategies have not been constructed.</p></div><div><h3>Case presentation</h3><p>We experienced a 23-year-old male with isolated chronic aseptic osteitis of the right proximal tibia, which was detected with magnetic resonance imaging and bone scintigraphy. We administered oral nonsteroidal anti-inflammatory drugs and local steroid injection, but his symptoms were not improved. Next, we administered oral methotrexate, which caused improvement effects, including decreased swelling and knee pain. In addition, the contrasted osteitis lesion in the proximal tibia demonstrated by magnetic resonance imaging completely disappeared.</p></div><div><h3>Conclusions</h3><p>Reports of osteitis in SAPHO syndrome resolved by methotrexate were rare. Although the effect of methotrexate on SAPHO syndrome was controversial, methotrexate should be considered for patients with refractory SAPHO syndrome before biologics.</p></div>","PeriodicalId":100743,"journal":{"name":"JOS Case Reports","volume":"3 2","pages":"Pages 105-110"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772964824000030/pdfft?md5=c55f6ab858475e62f1fa4702d2d9e2f0&pid=1-s2.0-S2772964824000030-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139539132","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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JOS Case Reports
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