Introduction
Endobronchial hamartoma is a rare benign tumor derived from peribronchial mesenchymal tissue. It can cause irreversible postobstructive pulmonary destruction with respiratory symptoms. Early diagnosis and treatment is very important. Traditionally, surgical resection has been considered the standard of treatment for endobronchial hamartoma. However, there is increasing experience using endoscopic treatment such as neodymium-doped yttrium aluminum garnet (Nd:YAG) laser and electrocautery for benign endobronchial tumor with a paucity of reported complications
1.
Bronchoscopic cryotherapy is a technique in which endobronchial tissue is destroyed by repeated freezing and thawing. This bronchoscopic technique is most often employed as a palliative therapy for malignant central airway obstruction with or without other modalities of endobronchial treatment
2,3.
We report two cases of endobronchial hamartoma, each diagnosed and definitively treated by cryotherapy via flexible bronchoscopy.
Discussion
Pulmonary hamartomas are the most common benign tumors of lung, with incidence 0.32% according to autopsy study
4. Pulmonary hamartomas divided into two groups according to their location: parenchymal hamartomas or endobronchial hamartomas. Endobronchial hamartomas have low frequency between 1.4% and 13.8% of all pulmonary hamartomas
5,6,7,8. Unlike the patients with parenchymal hamartomas, most patients with endobronchial hamartomas had at least one of respiratory complaints due to bronchial obstruction such as obstructive pneumonia, hemoptysis, cough, or dyspnea. Although endobronchial hamartomas are benign tumor with very low risk of malignancy and low rate of recurrence, early diagnosis and treatment is very important due to potential risk of bronchial obstruction, bleeding, and subsequent respiratory symptoms.
Although surgical resection has been considered the standard of treatment for endobronchial hamartomas, there is increasing case reports and case series using bronchoscopic treatment such as Nd:YAG laser and electrocautery with comparable therapeutic efficacy with surgical resection and few reported complications
1.
Cryotherapy is the application of extreme cold energy to diseased tissue, in which cells are destroyed by the formation of intracellular ice crystals. In 1968, the first case of the use of rigid cryoprobe through a rigid bronchoscope to relieve endobronchial obstruction by a tumor causing a postobstructive pneumonia was reported
9,10. Because of the need of general anesthesia and rigid bronchoscopy as well as development of other bronchoscopic treatment modalities such as laser resection, electrocautery, argon plasma coagulation, and photodynamic therapy, there was a relatively little interest in bronchoscopic cryotherapy until introduction of a flexible cryoprobe that allowed delivery through the flexible bronchoscope in 1994. Now, bronchoscopic cryotherapy is recognized as a useful endobronchial treatment modality in the palliative management for airway obstruction due to a malignancy
11,12. Bronchoscopic cryotherapy is also useful in management for airway obstruction due to a benign endobronchial lesion, inoperable microinvasive carcinoma, hemoptysis due to a visible lesion, and the extraction of foreign bodies.
For tumor cryodebridement, cryotherapy can be delivered through rigid or flexible bronchoscopy. After a full examination of bronchial segments, the tip of the bronchoscope is positioned 0.5-1.0 cm from the identified endobronchial lesion. Then, the cryoprobe inserted via the working channel of the bronchoscope. The cryoprobe is placed in direct contact with the tumor. Using the foot pedal, the bronchoscopist activates the cryoprobe. Cryogen will cool the probe tip to about -89℃. At this time, there are two techniques of cryodebridements: repeated thawing-freezing technique and pull-out technique
9,10. In a repeated thawing-freezing technique, freezing is continued for 30 seconds, after which the foot pedal is released, and passive thawing is allowed. This cycle is repeated an average of three cycles at each site of the tumor. Resultant necrotic tissue can be removed by suctioning, by biopsy forceps, or freezing the tissue to the cryoprobe. Repeated bronchoscopic examination is necessary for removal of necrotic tissue and clearing of secretion due to delayed sloughing of treated tissue. In a pull-out technique, the tip of the cryoprobe is cooled for 5-20 seconds. Then, the probe is pulled strongly, and the cryoprobe with frozen tissue attached to its tip is withdrawn along with the bronchoscope. The Pull-out technique, a newer method, has the potential advantage to decrease procedural time and achieve faster results with less need of repeated procedures
9. In our two cases, we selected a pull-out technique as a technique of cryotherapy for this reasons.
Recently, two diagnostic methods with cryotherapy were developed with improving diagnostic yield and safety: endobronchial biopsy with cryotherapy and fluoroscopy-guided transbronchial cryoprobe lung biopsy
13,14. During performing an endobronchial biopsy with cryoprobe, the cryoprobe is passed through the working channel of the bronchoscope and advanced 4 mm beyond the tip of the bronchoscope. Direct contact between the probe and the lesion is achieved. Tissue is frozen to the cryoprobe tip by activating the probe for approximately 5 seconds. While maintaining probe activation, the cryoprobe, with the frozen sample attached to it, is retracted back through the working channel of the bronchoscope. Alternatively, the cryoprobe with the frozen tissue attached to it can also be removed along with the flexible bronchoscope
9.
The effectiveness of cryotherapy is limited in long-segment, submucosal, and extrinsic tumors
9. Our cases were suitable for cryotherapy because endobronchial tumors narrowly attached the bronchus with stalk. We could relatively easily perform the endobronchial biopsy and removal of endobronchial hamartoma using cryotherapy via flexible bronchoscopy without complications. In case series of 521 patients, in-hospital mortality rate was 1%, all of which was due to respiratory failure
3. Three percent of patients developed respiratory distress after procedure which eventually resolved. Bleeding is usually mild and can generally be controlled by suction. During our procedures and postprocedural period, there was no notable complication except small amount of bleeding that was easily controlled by iced saline. Follow-up bronchoscopic examinations excluded residual or recurrent disease in our cases.
Although endobronchial cryotherapy has the disadvantages of potential need for repeated procedure, some delayed effects of treatment, and the relative resistance of certain benign tumors than other thermal techniques, this procedure has the advantage of a more favorable safety profiles and easier setup and procedural technique
9,10. We suggested cryotherapy with flexible bronchoscopy may be useful diagnostic and therapeutic modality in management of endobronchial tumor with few complications with or without other thermal modalities of endobronchial treatment.