Rustemeyer Jan, Günther Lutz, Junker Klaus, Thieme Volker, Busch Alexander, Okcu Yunus, Siegmund Birte Julia
Department of Oral and Maxillofacial Surgery and Plastic Operations, Klinikum Bremen-Mitte, School of Medicine of the University of Göttingen, Bremen, Germany.
Institute of Pathology, Klinikum Bremen-Mitte, School of Medicine of the University of Göttingen, Bremen, Germany.
J Maxillofac Oral Surg. 2021 Jun;20(2):219-226. doi: 10.1007/s12663-019-01324-8. Epub 2020 Jan 2.
Melanotic neuroectodermal tumour of infancy (MNTI) is a rare benign neoplasm. MNTI appears most often during the first year of life, arises predominantly in the maxilla and tends to recur. We discuss possible therapeutic options given in the literature and within our experience in three cases.
In our recent case, we used an intraoral approach to perform resection of the right-sided maxilla. Despite tumour-positive margins, there was no recurrence over the course of one year. In a previous case of MNTI, two recurrences occurred and 6 months after last resection patient received a rib graft for maxillary reconstruction. However, at the age of 7 years, the infant displayed severe maxillary hypoplasia. In a third case of MNTI, the patient was followed up after initial therapy for two decades and underwent multiple reconstruction procedures to achieve successful rehabilitation.
Surgical treatment of MNTI should respect vital anatomic structures to avoid gross mutilation. The need for extended and repetitive tumour resection in early childhood can lead to growth disturbances and to further multiple reconstruction procedures in adulthood. Because of the rarity of MNTI, an international database is warranted to evaluate therapies and clinical courses over decades.
婴儿黑色素性神经外胚层肿瘤(MNTI)是一种罕见的良性肿瘤。MNTI最常出现在生命的第一年,主要发生在上颌骨,且容易复发。我们根据文献及我们三例病例的经验讨论了可能的治疗选择。
在我们最近的病例中,我们采用口内入路切除右侧上颌骨。尽管切缘肿瘤阳性,但在一年的时间里没有复发。在之前一例MNTI病例中,出现了两次复发,最后一次切除术后6个月,患者接受了肋骨移植以进行上颌骨重建。然而,在7岁时,该婴儿出现了严重的上颌骨发育不全。在第三例MNTI病例中,患者在初始治疗后随访了20年,并接受了多次重建手术以实现成功康复。
MNTI的手术治疗应尊重重要的解剖结构以避免严重毁容。在儿童早期需要进行广泛且重复的肿瘤切除可能会导致生长发育障碍,并在成年期需要进一步进行多次重建手术。由于MNTI罕见,有必要建立一个国际数据库来评估数十年的治疗方法和临床病程。