Skip to main content
Erschienen in: World Journal of Surgical Oncology 1/2018

Open Access 01.12.2018 | Case report

Langerhans cell histiocytosis at L5 vertebra treated with en bloc vertebral resection: a case report

verfasst von: Lunhao Chen, Zhong Chen, Yue Wang

Erschienen in: World Journal of Surgical Oncology | Ausgabe 1/2018

Abstract

Background

Langerhans cell histiocytosis (LCH) in adult lumbar spine is extremely rare, and optimal treatments remain unclear. In literature, only a few cases of lumbar spine LCH were treated using surgery but en bloc vertebral resection has not been used.

Case presentation

A 50-year-old man presented with unbearable radiating pain at his right leg. Radiological studies revealed a solitary osteolytic lesion, which was moderately enhanced on contrast MR imaging and hyper-metabolic on PET/CT, at the right L5 vertebral body and arch. In biopsy, Langerhans cells were observed, but findings were insufficient to establish a diagnosis of LCH. A modified L5 en bloc vertebral resection via anterior and posterior approaches was performed to remove the right 2/3 portion of the L5 vertebra. The left 1/3 vertebral body and left pedicle of L5, which were not affected, were kept in situ to allow short instrumentation and reconstruction. His leg pain disappeared after the surgery, and a precise diagnosis of LCH was established after a throughout histological study of the removed vertebra. The patient further accepted 1 cycle of low-dose radiotherapy postoperatively. At 18-month follow-up, the lumbosacral spine was fused and no local reoccurrence was noticed.

Conclusions

For lumbar spine LCH, surgery should be considered if there are neurological symptoms or histological diagnosis is indefinite in biopsy. En bloc vertebral resection can be used to alleviate neurological symptoms and prevent local reoccurrence.

Background

Langerhans cell histiocytosis (LCH) is a proliferative disease that origins from dendritic cell family [1]. LCH is rare, with an estimated point prevalence of 1 case in 1.5 million [2]. LCH often involve multiple systems, and clinical presentations vary considerably [3, 4]. Osseous lesions are the most common findings in LCH, with approximately 60% of LCH patients had one or more lytic osseous lesions [3]. Typically, skull and femur are the most common bones involved. In rare case, osseous lesions occur in the spine, resulting in back pain, radiculopathy, or neurological deficits [5]. For spinal LCH, a standard treatment protocol is currently absent. Here, we report a rare case of LCH at the L5 vertebra which was treated with en bloc vertebral resection.

Case presentation

An otherwise healthy 50-year-old gentleman consulted us for his radiating pain at the right leg. The pain, which was triggered by 10-h driving 1 month ago, started from the right buttock and radiated down to the sole of the foot. The leg pain was rather severe, intolerable sometimes, and he cannot stand or walk when the pain attacked. He sought for treatment at a local hospital, and magnetic resonance (MR) imaging revealed an osseous lesion in the L5 vertebra. He was suspected to have lumbar metastasis and was referred to us for further treatment. He had no fever, no weight loss, and no bowel or bladder problems since he had the pain.
On physical examinations, he rated the leg pain as visual analogue scale (VAS) 7 points. His right straight leg raising test was positive. There was haphalgesia on his right calf, but no obvious sensation loss in the right leg. Manual muscle tests (MMT) revealed slightly decreased muscle power in his right tibialis anterior, gastrocnemius, and ankle dorsiflexors (grade IV+). His bilateral knee and ankle reflexes were normal. Pathological reflexes were negative for both legs.
On computed tomography (CT) images, the right portion of the L5 vertebra, including the vertebral body, pedicle, and transverse process, was destructed (Fig. 1a). Contrast CT revealed a mostly non-enhanced lytic lesion at the right L5 vertebral arch and body (Fig. 1b). The lesion, which was hypo-intense on T1-weighted (T1W) and hyper-intense on T2-weighted (T2W) sequences, mainly involved the right portion of vertebral body and arch and was moderately enhanced on gadolinium contrast sequence (Fig. 1cf). Positron emission tomography/computed tomography (PET/CT) revealed a single site of increased uptake of 18F-fluorodeoxyglucose (18F-FDG) at the right portion of the L5 vertebra (Fig. 2).
The patient underwent percutaneous needle biopsy. Histological studies reported the presence of some Langerhans cells in the tissue sample. Yet, histological evidence was not sufficient to make a conclusive diagnosis of LCH, and spine metastasis cannot be completely excluded due to some atypical cellular characteristics. The surgical team discussed with the patient and his family further treatment options, including repeated percutaneous biopsy, open biopsy, surgical curettage, vertebral resection, radiation therapy, chemotherapy, and some other possible interventions. After comprehensive discussions, the patient selected surgical removal of the vertebral lesion.
A modified L5 en bloc vertebral resection via anterior and posterior approaches was designed. As the lesion merely involved the right portion of the L5 vertebra, the left 1/3 portion were kept in situ to enhance segmental stability for the use of short instrumentation. First, a transabdominal approach was used to detach the right psoas and soft tissues from the L5 vertebra (Fig. 3a), remove the right portion of L4/5 and L5/S1 intervertebral discs, and sagittally split the L5 vertebral body at the junction between right 2/3 and left 1/3. Then, a posterior approach was used to perform laminectomy, and remove the disassociated L5 vertebral body (Fig. 3b, c), pedicle screw (L4, S1, and the left L5 pedicle), and cage (with autologous lamina bone graft) instrumentation (Fig. 4a, b). There was 1500 ml blood loss in the surgery.
The patient’s leg pain disappeared immediately after surgery. There was a generally decreased muscle power in his right leg (MMT grade IV) and consistent numbness in his right calf and foot. These symptoms, however, did not impair his mobility. With a brace, the patient walked independently 2 weeks after the surgery. A throughout histological study of the removed vertebra revealed numerous typical Langerhans cells, which were positive for S-100β and CD-1a (Fig. 5b, c). Ki-67 immunochemistry staining demonstrated that the Langerhans cells are active in proliferation (Fig. 5d). A pathological diagnosis of LCH was soundly established. The patient further accepted 1 cycle of low-dose radiotherapy (7 days) to eliminate potential remaining lesions in the surgical site. Mecobalamine was given for 12 months during his rehabilitation.
At 18-month follow-up, the patient had minor numbness in his ankle. His right calf was a bit thinner than the left, but no power weakness was noticed. He has returned to previous work and normal life 1 year ago. CT scan of the lumbar spine revealed that L4–S1 vertebrae were fused through the titanium mesh (Fig. 4c, d). No sign of reoccurrence was noticed in the lumbar spine.

Discussion

The current case highlighted a rare case of LCH in the L5 vertebra with nerve root compression which was treated with extensive surgical excision. Reportedly, only 4.1% of LCH osseous lesions occur in the lumbar spine [3], and involvement of spinal canal, nerve root or, paravertebral tissue is extremely rare [6]. In literature, no more than 10 cases of lumbar LCH were reported [5, 712], and four of them were treated with partial or complete surgical excision [8, 9, 11, 12]. In the present case, the intolerable neurological pain, indefinite diagnosis, and suspicious vertebral metastasis reported in biopsy led to a radical surgery to remove the lesion. Yet, the involvement of anterior and posterior portions of the L5 vertebra complicates the surgery. A modified en bloc vertebral resection via anterior and posterior approaches was performed, and the lumbosacral spine was reconstructed using short instrumentation. The patient had a favorable clinical outcome in short-term follow-up.
Routine radiological studies, such as X-ray, CT, and MR imaging, are able to identify osseous lesions but have little value in differentiating LCH from other osteolytic tumors. LCH typically exhibits hypo-intensity on T1W and hyper-intensity on T2W images and moderately enhancement on contrast MR images [12]. PET/CT is sensitive to detect hyper-metabolic lesions and multiple involvements of LCH. Specificities of these radiological approaches are low for the diagnosis of LCH, and none of them can lead to a definite diagnosis of LCH.
A precise diagnosis of LCH largely relies on biopsy and histological study [4]. Using percutaneous needle biopsy guided by CT or C-arm, reportedly, a definitive diagnosis can be established in 82–90% of cases of LCH [13, 14]. Still, there are a considerable number of cases that cannot be precisely diagnosed in needle biopsy. This may be due to either inadequate tissue sample obtained in needle biopsy or lack of typical cellular findings in histological study [14]. As in the current case, percutaneous needle biopsy failed to establish a conclusive diagnosis of LCH, though Langerhans cells were observed. According to World Health Organization classification of tumors of soft tissue and bone [15], LCH belongs to tumors of undefined neoplastic nature which may share some biological characteristics, such as osteolytic lesion, exophytic growth, and even distant metastasis, with some other bone neoplasms [3]. Moreover, it is noteworthy that LCH and other neoplasms sometimes may co-exist in a patient or even within a lesion [16, 17]. Approximately 4% of patients with LCH had concomitant neoplasms diagnosed at or after the time a diagnosis of LCH was established [3].
While there is no consensus on the management of LCH, a number of approaches, including surgery, chemotherapy, radiotherapy, glucocorticoid, monoclonal antibody, and even nonsteroidal anti-inflammatory drugs (NSAIDS), were used to treat LCH [5, 11, 18, 19]. For skeletal LCH, surgery should be considered if there is neurological involvement or histological diagnosis was not confident in biopsy [2022]. Surgical excision is an effective treatment for LCH, especially in patients with solitary bone lesions or neurological symptoms [3, 9]. In a case series of LCH in adults, 75% of who received marginal removal and 83% of who received simple curettage had no signs of local recurrence in an average of 8.5-year follow-up, which was better than those treated with chemotherapy or steroids (about 50% non-reoccurrence rate) [18].
Currently, the optimal treatments for spinal LCH remain controversial. While most cases of spinal LCH were treated conservatively, surgical curettage or excision was also reported [6, 9, 11]. Occasionally, solidary lumbar LCH was treated with hemi-vertebral resection through a posterolateral approach [9]. En bloc vertebral resection is a developed surgery which has been proven to be efficacious in treating solitary spine tumors [23, 24], and particularly can reduce the chance of local recurrence [25]. To our knowledge, this is the first time that en bloc technique was used to treat spinal LCH. In this special case, instead of a traditional en bloc vertebral resection, we kept the left 1/3 L5 vertebra to reduce surgical time, maintain segmental stability, and shorten spinal instrumentation. As is the case, the patient was mobile shortly after the surgery, and solid lumbosacral fusion was achieved on time.
One may doubt if such a radical surgery is too aggressive for the current patient. It is possible that the patient can be managed using chemotherapy or radiotherapy, if a precise diagnosis of LCH can be established in biopsy. Yet, it is not clear if symptoms of nerve root compression can be relieved using non-surgical treatments. While surgery can quickly alleviate pain symptoms, radical removal may be better than local excision to achieve disease-free survival.

Conclusions

We reported a rare case of adult LCH in the L5 vertebra with neurological compression. The patient was successfully treated using a modified en bloc vertebral resection. Although aggressive, en bloc vertebral resection was effective to quickly relieve pain symptoms and prevent local reoccurrence in treating spinal LCH.

Funding

This work was partially supported by the National Natural Science Foundation of China (NSFC; No. 81772382) and Science Technology Department of Zhejiang Province (No. 2014C33192).
Not applicable.
Written informed consent was obtained from the patient for the publication of this case presentation and accompanying images.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
1.
Zurück zum Zitat Willman CL, Busque L, Griffith BB, Favara BE, McClain KL, Duncan MH, Gilliland DG. Langerhans’-cell histiocytosis (histiocytosis X)—a clonal proliferative disease. N Engl J Med. 1994;331:154–60.CrossRefPubMed Willman CL, Busque L, Griffith BB, Favara BE, McClain KL, Duncan MH, Gilliland DG. Langerhans’-cell histiocytosis (histiocytosis X)—a clonal proliferative disease. N Engl J Med. 1994;331:154–60.CrossRefPubMed
2.
Zurück zum Zitat Zhong WQ, Jiang L, Ma QJ, Liu ZJ, Liu XG, Wei F, Yuan HS, Dang GT. Langerhans cell histiocytosis of the atlas in an adult. Eur Spine J. 2010;19:19–22.CrossRefPubMed Zhong WQ, Jiang L, Ma QJ, Liu ZJ, Liu XG, Wei F, Yuan HS, Dang GT. Langerhans cell histiocytosis of the atlas in an adult. Eur Spine J. 2010;19:19–22.CrossRefPubMed
3.
Zurück zum Zitat Howarth DM, Gilchrist GS, Mullan BP, Wiseman GA, Edmonson JH, Schomberg PJ. Langerhans cell histiocytosis: diagnosis, natural history, management, and outcome. Cancer. 1999;85:2278–90.CrossRefPubMed Howarth DM, Gilchrist GS, Mullan BP, Wiseman GA, Edmonson JH, Schomberg PJ. Langerhans cell histiocytosis: diagnosis, natural history, management, and outcome. Cancer. 1999;85:2278–90.CrossRefPubMed
5.
Zurück zum Zitat Hassan BW, Moon BJ, Kim YJ, Kim SD, Choi KY, Lee JK. Langerhans cell histiocytosis in the adult lumbar spine: case report. Spring. 2016;5:1398.CrossRef Hassan BW, Moon BJ, Kim YJ, Kim SD, Choi KY, Lee JK. Langerhans cell histiocytosis in the adult lumbar spine: case report. Spring. 2016;5:1398.CrossRef
6.
Zurück zum Zitat Acciarri N, Paganini M, Fonda C, Gaist G, Padovani R. Langerhans cell histiocytosis of the spine causing cord compression: case report. Neurosurgery. 1992;31:965–8.CrossRefPubMed Acciarri N, Paganini M, Fonda C, Gaist G, Padovani R. Langerhans cell histiocytosis of the spine causing cord compression: case report. Neurosurgery. 1992;31:965–8.CrossRefPubMed
7.
Zurück zum Zitat Demirci I. Adult eosinophilic granuloma of the lumbar spine with atypical dissemination. Case report: a long-term follow-up. Zentralbl Neurochir. 2004;65:84–7.CrossRefPubMed Demirci I. Adult eosinophilic granuloma of the lumbar spine with atypical dissemination. Case report: a long-term follow-up. Zentralbl Neurochir. 2004;65:84–7.CrossRefPubMed
8.
Zurück zum Zitat Nakamura H, Nagayama R. Eosinophilic granuloma presenting with local osteolysis in an adult lumbar spine. J Clin Neurosci. 2008;15:1398–400.CrossRefPubMed Nakamura H, Nagayama R. Eosinophilic granuloma presenting with local osteolysis in an adult lumbar spine. J Clin Neurosci. 2008;15:1398–400.CrossRefPubMed
9.
Zurück zum Zitat Bilge T, Barut S, Yaymaci Y, Alatli C. Solitary eosinophilic granuloma of the lumbar spine in an adult. Case Rep Paraplegia. 1995;33:485–7. Bilge T, Barut S, Yaymaci Y, Alatli C. Solitary eosinophilic granuloma of the lumbar spine in an adult. Case Rep Paraplegia. 1995;33:485–7.
10.
Zurück zum Zitat Bavbek M, Atalay B, Altinors N, Caner H. Spontaneous resolution of lumbar vertebral eosinophilic granuloma. Acta Neurochir. 2004;146:165–7.CrossRefPubMed Bavbek M, Atalay B, Altinors N, Caner H. Spontaneous resolution of lumbar vertebral eosinophilic granuloma. Acta Neurochir. 2004;146:165–7.CrossRefPubMed
11.
Zurück zum Zitat Feng F, Tang H, Chen H, Jia P, Bao L, Li JJ. Percutaneous vertebroplasty for Langerhans cell histiocytosis of the lumbar spine in an adult: case report and review of the literature. Exp Ther Med. 2013;5:128–32.CrossRefPubMed Feng F, Tang H, Chen H, Jia P, Bao L, Li JJ. Percutaneous vertebroplasty for Langerhans cell histiocytosis of the lumbar spine in an adult: case report and review of the literature. Exp Ther Med. 2013;5:128–32.CrossRefPubMed
12.
Zurück zum Zitat Paxinos O, Delimpasis G, Makras P. Adult case of Langerhans cell histiocytosis with single site vertebral involvement. J Musculoskelet Neuronal Interact. 2011;11:212–4. quiz 4PubMed Paxinos O, Delimpasis G, Makras P. Adult case of Langerhans cell histiocytosis with single site vertebral involvement. J Musculoskelet Neuronal Interact. 2011;11:212–4. quiz 4PubMed
13.
Zurück zum Zitat Yasko AW, Fanning CV, Ayala AG, Carrasco CH, Murray JA. Percutaneous techniques for the diagnosis and treatment of localized Langerhans-cell histiocytosis (eosinophilic granuloma of bone). J Bone Joint Surg Am. 1998;80:219–28.CrossRefPubMed Yasko AW, Fanning CV, Ayala AG, Carrasco CH, Murray JA. Percutaneous techniques for the diagnosis and treatment of localized Langerhans-cell histiocytosis (eosinophilic granuloma of bone). J Bone Joint Surg Am. 1998;80:219–28.CrossRefPubMed
14.
Zurück zum Zitat Huang WD, Yang XH, Wu ZP, Huang Q, Xiao JR, Yang MS, Zhou ZH, Yan WJ, Song DW, Liu TL, Jia NY. Langerhans cell histiocytosis of spine: a comparative study of clinical, imaging features, and diagnosis in children, adolescents, and adults. Spine J. 2013;13:1108–17.CrossRefPubMed Huang WD, Yang XH, Wu ZP, Huang Q, Xiao JR, Yang MS, Zhou ZH, Yan WJ, Song DW, Liu TL, Jia NY. Langerhans cell histiocytosis of spine: a comparative study of clinical, imaging features, and diagnosis in children, adolescents, and adults. Spine J. 2013;13:1108–17.CrossRefPubMed
15.
Zurück zum Zitat Fletcher CD, Bridge J A., Hogendoorn P. C., Mertens F. WHO classification of tumors of soft tissue and bone. IARC. 2013:356–7. Fletcher CD, Bridge J A., Hogendoorn P. C., Mertens F. WHO classification of tumors of soft tissue and bone. IARC. 2013:356–7.
16.
Zurück zum Zitat Egeler RM, Neglia JP, Puccetti DM, Brennan CA, Nesbit ME. Association of Langerhans cell histiocytosis with malignant neoplasms. Cancer. 1993;71:865–73.CrossRefPubMed Egeler RM, Neglia JP, Puccetti DM, Brennan CA, Nesbit ME. Association of Langerhans cell histiocytosis with malignant neoplasms. Cancer. 1993;71:865–73.CrossRefPubMed
17.
Zurück zum Zitat Egeler RM, Neglia JP, Arico M, Favara BE, Heitger A, Nesbit ME. Acute leukemia in association with Langerhans cell histiocytosis. Med Pediatr Oncol. 1994;23:81–5.CrossRefPubMed Egeler RM, Neglia JP, Arico M, Favara BE, Heitger A, Nesbit ME. Acute leukemia in association with Langerhans cell histiocytosis. Med Pediatr Oncol. 1994;23:81–5.CrossRefPubMed
18.
Zurück zum Zitat Cantu MA, Lupo PJ, Bilgi M, Hicks MJ, Allen CE, McClain KL. Optimal therapy for adults with Langerhans cell histiocytosis bone lesions. PLoS One. 2012;7:e43257.CrossRefPubMedPubMedCentral Cantu MA, Lupo PJ, Bilgi M, Hicks MJ, Allen CE, McClain KL. Optimal therapy for adults with Langerhans cell histiocytosis bone lesions. PLoS One. 2012;7:e43257.CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Kelly KM, Pritchard J. Monoclonal antibody therapy in Langerhans cell histiocytosis—feasible and reasonable? Br J Cancer Suppl. 1994;23:S54–5.PubMedPubMedCentral Kelly KM, Pritchard J. Monoclonal antibody therapy in Langerhans cell histiocytosis—feasible and reasonable? Br J Cancer Suppl. 1994;23:S54–5.PubMedPubMedCentral
20.
Zurück zum Zitat Sadashiva N, Rajalakshmi P, Mahadevan A, Vazhayil V, Rao KN, Somanna S. Surgical treatment of Langerhans cell histiocytosis of cervical spine: case report and review of literature. Childs Nerv Syst. 2016;32:1149–52.CrossRefPubMed Sadashiva N, Rajalakshmi P, Mahadevan A, Vazhayil V, Rao KN, Somanna S. Surgical treatment of Langerhans cell histiocytosis of cervical spine: case report and review of literature. Childs Nerv Syst. 2016;32:1149–52.CrossRefPubMed
21.
Zurück zum Zitat Lu GH, Li J, Wang XB, Wang B, Phan K. Surgical treatment based on pedicle screw instrumentation for thoracic or lumbar spinal Langerhans cell histiocytosis complicated with neurologic deficit in children. Spine J. 2014;14:768–76.CrossRefPubMed Lu GH, Li J, Wang XB, Wang B, Phan K. Surgical treatment based on pedicle screw instrumentation for thoracic or lumbar spinal Langerhans cell histiocytosis complicated with neurologic deficit in children. Spine J. 2014;14:768–76.CrossRefPubMed
22.
Zurück zum Zitat Huang W, Yang X, Cao D, Xiao J, Yang M, Feng D, Huang Q, Wu Z, Zheng W, Jia L, Wu S. Eosinophilic granuloma of spine in adults: a report of 30 cases and outcome. Acta Neurochir. 2010;152:1129–37.CrossRefPubMed Huang W, Yang X, Cao D, Xiao J, Yang M, Feng D, Huang Q, Wu Z, Zheng W, Jia L, Wu S. Eosinophilic granuloma of spine in adults: a report of 30 cases and outcome. Acta Neurochir. 2010;152:1129–37.CrossRefPubMed
23.
Zurück zum Zitat Boriani S, Biagini R, De Iure F, Bertoni F, Malaguti MC, Di Fiore M, Zanoni A. En bloc resections of bone tumors of the thoracolumbar spine. A preliminary report on 29 patients. Spine. 1996;21:1927–31.CrossRefPubMed Boriani S, Biagini R, De Iure F, Bertoni F, Malaguti MC, Di Fiore M, Zanoni A. En bloc resections of bone tumors of the thoracolumbar spine. A preliminary report on 29 patients. Spine. 1996;21:1927–31.CrossRefPubMed
24.
Zurück zum Zitat Boriani S, Biagini R, Andreoli I, De Iure F, Campanacci L, Dimitri S, Gamberini G. Resection of the vertebral arch in the treatment of neoplasms of the spine. Chir Organi Mov. 1995;80:183–9.PubMed Boriani S, Biagini R, Andreoli I, De Iure F, Campanacci L, Dimitri S, Gamberini G. Resection of the vertebral arch in the treatment of neoplasms of the spine. Chir Organi Mov. 1995;80:183–9.PubMed
25.
Zurück zum Zitat Collaud S, Fadel E, Schirren J, Yokomise H, Bolukbas S, Dartevelle P, Keshavjee S, Waddell TK, de Perrot M. En bloc resection of pulmonary sulcus non-small cell lung cancer invading the spine: a systematic literature review and pooled data analysis. Ann Surg. 2015;262:184–8.CrossRefPubMed Collaud S, Fadel E, Schirren J, Yokomise H, Bolukbas S, Dartevelle P, Keshavjee S, Waddell TK, de Perrot M. En bloc resection of pulmonary sulcus non-small cell lung cancer invading the spine: a systematic literature review and pooled data analysis. Ann Surg. 2015;262:184–8.CrossRefPubMed
Metadaten
Titel
Langerhans cell histiocytosis at L5 vertebra treated with en bloc vertebral resection: a case report
verfasst von
Lunhao Chen
Zhong Chen
Yue Wang
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
World Journal of Surgical Oncology / Ausgabe 1/2018
Elektronische ISSN: 1477-7819
DOI
https://doi.org/10.1186/s12957-018-1399-1

Weitere Artikel der Ausgabe 1/2018

World Journal of Surgical Oncology 1/2018 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

CME: 2 Punkte

Prof. Dr. med. Gregor Antoniadis Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

CME: 2 Punkte

Dr. med. Benjamin Meyknecht, PD Dr. med. Oliver Pieske Das Webinar S2e-Leitlinie „Distale Radiusfraktur“ beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

CME: 2 Punkte

Dr. med. Mihailo Andric
Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.