Tracheostomy for the pediatric patient with fibrodysplasia ossificans progressiva: a case report

A 12-year-old boy (height: 109 cm; weight: 21 kg) with FOP was referred to our hospital for tracheostomy. He had undergone orotracheal intubation 2 months prior owing to restrictive ventilatory impairment caused by severe deformities and contractures of the neck, thorax, and spine.

The patient was diagnosed with FOP at the age of one. The ectopic ossification and deformation of his cervical scapulothoracic cage occurred and progressed without intellectual disability, difficulties in walking, or problems attending school. He required oxygen administration from the age of nine years because of restrictive ventilation failure. However, ectopic ossification and his cervical scapulothoracic deformity rapidly progressed. At the age of 12, he developed severe dyspnea requiring emergency oral intubation and mechanical ventilation.

We were concerned that many surgical procedures, including tracheostomy, were typically contraindicated for patients with FOP, because they could lead to ectopic ossifications. Therefore, we visited the patient at the referring hospital for preliminary assessment. Physical examination revealed that the patient could not be placed in the supine position. In addition, we observed that the space in his anterior neck was insufficient for the surgery because the patient could not stretch his neck (Fig. 1). Based on these findings, tracheostomy was considered extremely difficult for him.

Fig. 1figure 1

Limited space in the anterior neck due to thoracic trunk deformity at initial oral intubation

Very few cases of tracheostomy performed in patients with FOP during childhood have been reported. While we were researching surgical options for our patient, unscheduled extubation was performed twice within 4 weeks. Each reintubation after the events was very difficult. Furthermore, the patient had difficult experiences such as flare-ups, atelectasis, and pneumonia. He endured great emotional distress and hoped for tracheostomy as soon as possible. After thorough research and several preoperative meetings, we decided to perform the procedure.

Two weeks before surgery, the patient was transferred to our hospital for preoperative evaluation and preparation. We examined the neck and thorax deformity under general anesthesia and changed the intubation route from oral to nasal. Three-dimensional computed tomography (3D-CT) was performed to facilitate the selection of his tracheostomy tube (Fig. 2). Given the patient’s severe scoliosis and contracture, the shape and condition of his neck and chest and the position of his trachea were significantly different from those of a healthy child. Therefore, preoperative 3D-CT was used to clearly visualize the space from the anterior chest wall to the neck, measure the distance from the neck skin to the anterior tracheal wall, and determine the meandering course of the trachea in his daily posture. These insights provide valuable in preparing a tracheal tube tailored to the patient’s specific needs, accounting for the appropriate thickness, length, and shape in advance. Ensuring the insertion of a suitable tube during tracheostomy was also important for the patient’s comfort in the early postoperative period.

Fig. 2figure 2

Three-dimensional computed tomography (3D-CT) before tracheostomy

Although the patient was administered high-dose steroids for preventing flare-ups, we performed the tracheostomy procedure cautiously. Unlike typical tracheostomy, the trachea was far from the skin because the patient’s neck could not be tilted. A horizontal incision was made on the skin at the level of the inferior border of the cricoid cartilage, then the anterior cervical musculature was divided along the midline gently. The blood vessels in the thyroid isthmus were separated from the tracheal surface as far as possible without damaging thyroid tissues. An inverted U-shaped incision was made in the tracheal wall from the lower part of the cricoid cartilage to the upper part of the second tracheal cartilage. Thereafter, the skin was sutured to the entire circumference of the tracheal hole. This surgical method, involving suturing the trachea to the skin, especially closing the mediastinal side with a tracheal wall flap, allowed for safe reinsertion immediately after surgery, even if the tube was removed unexpectedly. To prevent additional chronic trauma, we did not suture the tube to the skin. In addition, his neck and shoulder does not move freely, so even if the cannula is not tightly secured to his neck, unplanned removal is unlikely unless the cannula is intentionally pulled out. We performed bronchoscopy to confirm a suitable tube for the patient’ deformed trachea and finally selected a 5.5 Fr cuffed tracheostomy tube (Figs. 3 and 4).

Fig. 3figure 3

Anterior neck appearance during tracheostomy under general anesthesia. a, b Anterior neck space is available in maximum neck extension position; c A 5.5 Fr cuffed tracheostomy tube is inserted after tracheostomy

Fig. 4figure 4

Schematic diagram showing an inverted U-shaped tracheal wall incision and the anterior tracheal wall flap. a Inverted U-shaped tracheal wall incision. The dashed circle indicates the surgical field of view. T: thyroid cartilage, C: cricoid cartilage, 1–3: tracheal cartilage; b Anterior tracheal wall flap, 1.2: tracheal cartilage (lateral view)

The patient developed postoperative posterior reversible encephalopathy syndrome (PRES), which appeared to be caused by stress associated with long-term intubation, requiring sedation and mechanical ventilation for 2 days. He had high blood pressure due to PRES for a week, without experiencing other complications. Oral intake was initiated on postoperative day 5, then he recovered to a good state in terms of activities of daily living. On postoperative day 7, the patient was transferred to the previous hospital and discharged after a period of physical therapy.

One month after the surgery, the patient was placed on a ventilator at night only. The tracheostomy cannula was replaced with the cuffless one, consequently, he could breathe and speak easily. The postoperative CT showed no ossification at the surgical site or abnormal cannula placement (Fig. 5). The patient gradually regained the ability to speak and could return to his school. His ability to resume his daily activities indicated that the tracheostomy improved his quality of life (QOL).

Fig. 5figure 5

Computed tomography (CT) image at 1 month after tracheostomy. CT shows no ossification at the surgical site or abnormalities in cannula placement

At the time of this report, the patient was 16 years old. He is a high school student and has lived with his family as he wanted before the surgery. Since the patient is growing with a progressive disease, several problems have been encountered. His ventilatory impairment progressed to the point where he needed a ventilator almost all day long, and required high airway pressure with a cuffed cannula to maintain breathing during sleep. Currently, it is difficult for him to undergo cannula replacement without general anesthesia due to pain and fear of dyspnea.

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