- Case report
- Open Access
- Open Peer Review
Hyperbaric oxygen therapy for a refractory skin ulcer after radical mastectomy and radiation therapy: a case report
Journal of Medical Case Reports volume 11, Article number: 5 (2017)
Radiation therapy is performed as an adjuvant therapy when indicated following surgical resection of malignant tumors. However, radiation exposure induces acute or chronic dermatitis, depending on the radiation dose, interval, tissue volume, or irradiated area of the body. Radiation-induced skin ulcers and osteomyelitis of the underlying bone are intractable late-stage complications of radiation therapy, and often require reconstructive surgery to cover exposed tissue. Hyperbaric oxygen therapy has been suggested as a treatment for delayed radiation injury with soft tissue and bony necrosis.
A 74-year-old Japanese female underwent left radical mastectomy for breast cancer (T3N3M0, stage IIIB) in 1987. Radiation therapy was initiated 6 weeks after the surgery. She received telecobalt-60 in a total dose of 50 Gy with 25 fractions to the left supraclavicular, parasternal and left axillary regions, and electron treatment (9 MeV) in a total dose of 50 Gy in 25 fractions to the left chest wall. After irradiation, her skin became thinner and more fragile on the left chest wall, but no severe infections were observed. She noticed a small ulcer that repeatedly healed and recurred in 2000. She visited the hospital where she received radiation therapy and was treated for a skin ulcer on the left chest wall in December 2012. A fistula developed and then pus was discharged in January 2013. She was referred to the hyperbaric medical center in February 2013, and the fistula (1.5 × 3 cm) with pus discharge was observed. She was diagnosed with a late-onset radiation-induced skin ulcer that developed 25 years after radical mastectomy. HBO2 (2.5 atmospheres absolute with 100% oxygen for 60 minutes) was indicated for the refractory ulcer and osteomyelitis of the ribs. The patient was treated with HBO2 a total of 101 times over the course of 1 year and completely recovered.
Hyperbaric oxygen therapy can be performed safely for even more than 100 sessions in patients with radiation-induced skin ulcers and osteomyelitis. Hyperbaric oxygen therapy can be considered as an alternative, conservative treatment when surgical resection for late-onset, radiation-induced skin ulcers is not indicated because of fragile skin in the irradiated areas.
Recently, the use of fluoroscopic procedures has increased as a result of advances in interventional radiology such as cardiac catheterization or intravascular surgery, which use such procedures. However, radiation exposure can cause dermopathies, including refractory skin ulcers . Guidelines for radiation exposure were established by the Society of Interventional Radiology in 2009 . Japanese guidelines were also established by the Japanese Society for Therapeutic Radiology and Oncology in 2012 (http://www.jastro.or.jp/guideline/child.php?eid=00007). Radiation therapy is widely recognized as a curative treatment for multiple types of cancers, including prostate, head and neck, lung, uterine, esophageal, and brain cancers, as well as lymphomas. In breast cancer, radiation therapy is used primarily as an adjuvant treatment following surgery . However, high-dose radiation exposure of thin soft tissue often causes acute or delayed skin ulcers. In addition, osteomyelitis of the ribs becomes intractable when chest skin ulcers are present. In such cases, chest wall reconstruction might finally be needed in addition to aggressive skin or rib resection .
Hyperbaric oxygen therapy (HBO2) has been suggested for treatment of delayed radiation injury with soft tissue and bony necrosis . We report a case of a patient with refractory skin ulcer of the left chest wall that developed after radical mastectomy and radiation therapy for breast cancer, which was successfully treated with HBO2.
A 74-year-old Japanese woman underwent left radical mastectomy in 1987 for breast cancer with a size of 6 × 4 cm in the upper outer quadrant (T3N3M0, stage IIIB). Tamoxifen was administered in addition to tegafur and OK-432 as an adjuvant chemotherapy after the surgery. The tumor was negative for both estrogen receptor and progesterone receptor and was evaluated as N2b. Radiation therapy was initiated 6 weeks after the surgery. Initially, the patient received telecobalt-60 treatment, comprising 24 Gy in 12 fractions (days) to the supraclavicular and parasternal regions and 14 Gy in 7 fractions (days) to the left axilla, because of delayed wound healing after the surgery. Her wound was completely healed 15 days after the radiation treatment. The cobalt-60 treatment was resumed, comprising 26 Gy in 13 fractions to the supraclavicular and parasternal regions and 36 Gy in 18 fractions to the left axilla for 27 days, resulting in a total of 50 Gy in 25 fractions in each region. At the same time, electron treatment (9 MeV) to the left chest wall was started such that it did not overlap with the treatment of the supraclavicular, parasternal, and axillary regions. After the patient had received 44 Gy in 22 fractions at 32 days, skin redness and swelling occurred, and the treatment was stopped. After a 1-month rest period, 3 additional fractions were performed to provide a total of 50 Gy in 25 fractions. At that time, a keloidal change corresponding to the electron treatment area on the patient’s left chest wall was noted; her skin became thinner and more fragile, but no severe infections were observed.
The patient noticed a small ulcer at the beginning of 2000, but the ulcer healed over time without treatment. She visited the hospital where she received radiation therapy in December 2012, and at that time she was treated with cadexomer iodine ointment for a skin ulcer on the left chest wall. A fistula eventually developed, and pus discharging from the fistula was observed in January 2013. She was referred to the hyperbaric medical center in February 2013. The fistula (1.5 × 3 cm) with pus discharge on her left chest wall was noted at her first visit (Fig. 1a). The skin around the lesion showed redness and swelling with a keloidal change. The pus discharge was synchronized to her respiratory rhythm, and a bacterial identification test result was positive for Staphylococcus aureus. A pulmonary function test revealed pulmonary restriction (percent predicted vital capacity [%VC] 60.6 %, percent predicted forced expiratory volume in 1 second [FEV1%] 80.2 %). Chest radiography showed cardiac enlargement. Chest computed tomography (CT) showed no cystic lesions, and the fistula located on the left chest wall did not invade the thorax (Fig. 1b). The patient was diagnosed with a late-onset, radiation-induced skin ulcer that developed 25 years after radical mastectomy. HBO2 was indicated for the refractory ulcer and osteomyelitis of the ribs. Her medical history included acute myocardial infarction and a stent implanted in 2003. She was instructed to communicate any problems including otalgia, ear fullness, hearing loss, tinnitus, vertigo, and dizziness to a physician at the hyperbaric medical center.
HBO2 therapy was started in March 2013 after written informed consent was obtained. A multiplace hyperbaric chamber (NHC-412-A; Nakamura Tekko-Sho K.K., Tokyo, Japan) was pressurized up to 2.5 atmospheres absolute (ATA) with 100 % oxygen delivered through a mask. The duration of each treatment session was 105 minutes, including 15 minutes of compression at the beginning and 20 minutes of decompression at the end of treatment. The patient tolerated the HBO2 protocol without any adverse effects, despite her pulmonary restriction and cardiac enlargement. After 25 sessions over the course of 3 months, granulation tissue was observed around the margin of the ulcer, but massive pus discharge was still noted (Fig. 2a). At this time, a physician suggested that the ulcer be washed with tap water once daily. Granulation tissue gradually increased and pus discharge diminished without use of antibiotics (Fig. 2b, c). After 86 sessions over the course of 11 months, epithelialization was observed and pus discharge disappeared (Fig. 2d). A pulmonary function test at this time still revealed pulmonary restriction (%VC 58.6 %, FEV1% 85.2 %), with no remarkable change compared with previous findings. After 101 sessions over a period of 1 year, the ulcer was considered to be healed. The patient no longer had to cover her skin wound and was able to bathe after the treatment. At a follow-up visit 6 months after the completion of HBO2 therapy, no recurrence of skin ulceration was noted (Fig. 3a). Chest CT was performed to evaluate the further development of abnormal lesions. We found that osteomyelitis of the ribs had developed following the formation of the skin ulcer compared with the previous CT. A rib defect was observed on three-dimensional chest CT (Fig. 3b). The rib defect was managed conservatively because the patient’s symptoms were limited to left chest pain in her daily life.
Acute- and late-onset skin reactions are adverse effects of radiation therapy and are categorized using several scoring systems [6, 7]. Delayed changes usually develop within 4–6 months, and the irradiated skin could have an increased risk of infection, delayed healing, wound dehiscence, fistula formation, and wound necrosis . Radiation-induced skin ulcers can become intractable as a result of improper wound healing, infection, or both. In our patient, thinning of the chest wall by resection of breast muscle and the irradiation protocol contributed to the formation of an intractable ulcer. According to the patient’s history of dermatitis during radiation therapy, the skin ulcer recurred 25 years after treatment. The patient’s skin was already red and fragile, and the ulcer had become intractable, but the infection was localized around the ulcer before her hospital visit. For these reasons, HBO2 was considered to be the best conservative treatment option. In the case of large skin ulcers with massive infection and bone necrosis, surgical treatment, including resection of the ulcer, sternum, and ribs with osteomyelitis followed by reconstruction of the chest wall using skin or muscle flaps, should be considered [9, 10]. Malignancy also should be considered in the differential diagnosis, and a biopsy should be performed to rule out a second malignancy in the radiated field . In our patient, carcinogenesis was not suspected on the basis of the gross appearance of the skin and radiographic findings before starting HBO2. We examined the appearance of the skin at least every 2 weeks during the HBO2 sessions to detect nontypical wound healing.
HBO2 involves breathing pure oxygen at an ambient pressure higher than atmospheric pressure. The worldwide standard HBO2 protocol is to apply 2.0–2.8 ATA for 60–90 minutes with pressurized air or oxygen inside the chamber . HBO2 is thought to have complex effects on immunity, oxygen transport, and hemodynamics, resulting in favorable therapeutic effects by reducing hypoxia and edema as well as enabling normal host responses to infection and ischemia [12, 13]. Indications for HBO2 according to the Undersea and Hyperbaric Medical Society include arterial insufficiency (enhancement of healing for select problematic wounds); refractory osteomyelitis; and delayed, radiation-induced soft tissue injury or bone necrosis . There are several contraindications for HBO2. Absolute contraindications include doxorubicin treatment (because of cardiac toxicity), mafenide acetate treatment (because of central vasoconstriction), and untreated pneumothorax . According to authors of a Cochrane review of chronic wounds, HBO2 improved healing in the short term but not with long-term follow-up . In experimental studies, HBO2 treatment led to proliferation of bovine aortic endothelial cells and human skin fibroblasts in vitro as well as accelerated wound epithelialization and neovascularization in mouse ears [17, 18]. Clinically, a positive correlation has been reported between tissue oxygenation and various markers of wound healing. These results support the efficacy of HBO2 .
Our patient’s case met the indications for HBO2, and she had no recurrence at least 6 months after treatment. The average total number of HBO2 sessions for chronic wounds is in the range of 30–40 . Our patient underwent 101 sessions over a period of 1 year. However, cases of radiation-induced injury require a greater number of sessions (30–60) than those involving chronic wounds . In particular, radiation-induced ulcers of the chest wall with bone necrosis often require more frequent HBO2 sessions as well as surgical intervention . In one case report, necrotic lesions induced by accidental radiation exposure improved after 140 sessions of HBO2, without any adverse effects . Thus, delayed, radiation-induced injury of the chest wall can be treated successfully with more than 100 sessions of HBO2. However, long-term studies are needed to determine whether surgical intervention will eventually be required.
We treated a patient with refractory skin ulcer on the left chest wall that developed 25 years after radical mastectomy and radiation therapy for breast cancer. The patient was successfully treated with HBO2 a total of 101 times over the course of 1 year without any adverse effects.
- FEV1% :
Percent predicted forced expiratory volume in 1 second
- HBO2 :
Hyperbaric oxygen therapy
Percent predicted vital capacity
Olascoaga A, Vilar-Compte D, Poitevin-Chacón A, Contreras-Ruiz J. Wound healing in radiated skin: pathophysiology and treatment options. Int Wound J. 2008;5:246–57.
Stecker MS, Balter S, Towbin RB, Miller DL, Vañó E, Bartal G, et al. Guidelines for patient radiation dose management. J Vasc Interv Radiol. 2009;20(7 Suppl):S263–73.
Senkus E, Kyriakides S, Ohno S, Penault-Llorca F, Poortmans P, Rutgers E, et al. Primary breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2015;26 Suppl 5:v8–30.
Beahm EK, Chang DW. Chest wall reconstruction and advanced disease. Semin Plast Surg. 2004;18:117–29.
Feldmeier JJ, Heimbach RD, Davolt DA, Court WS, Stegmann BJ, Sheffield PJ. Hyperbaric oxygen as an adjunctive treatment for delayed radiation injury of the chest wall: a retrospective review of twenty-three cases. Undersea Hyperb Med. 1995;22:383–93.
Porock D. Factors influencing the severity of radiation skin and oral mucosal reactions: development of a conceptual framework. Eur J Cancer Care (Engl). 2002;11:33–43.
Ryan JL. Ionizing radiation: the good, the bad, and the ugly. J Invest Dermatol. 2012;132:985–93.
Wang J, Boerma M, Fu Q, Hauer-Jensen M. Radiation responses in skin and connective tissues: effect on wound healing and surgical outcome. Hernia. 2006;10:502–6.
Arnold PG, Pairolero PC. Surgical management of the radiated chest wall. Plast Reconstr Surg. 1986;77:605–12.
Fujioka M. Surgical reconstruction of radiation injuries. Adv Wound Care (New Rochelle). 2014;3:25–37.
Granick MS, Larson DL, Solomon MP. Radiation-related wounds of the chest wall. Clin Plast Surg. 1993;20:559–71.
Grim PS, Gottlieb LJ, Boddie A, Batson E. Hyperbaric oxygen therapy. JAMA. 1990;263:2216–20.
Gill AL, Bell CN. Hyperbaric oxygen: its uses, mechanisms of action and outcomes. QJM. 2004;97:385–95.
Weaver LK. Undersea and Hyperbaric Medical Society Hyperbaric Oxygen Committee. Hyperbaric oxygen therapy indications: the Hyperbaric Oxygen Therapy Committee report. 13th ed. North Palm Beach: Best Publishing; 2014.
Kindwall EP, Whelan HT. Contraindications and side effects to hyperbaric oxygen treatment. In: Kindwall EP, Whelan HT, editors. Hyperbaric medicine practice. 3rd ed. North Palm Beach: Best Publishing; 2008. p. 273–88.
Kranke P, Bennett MH, Martyn-St James M, Schnabel A, Debus SE, Weibel S. Hyperbaric oxygen therapy for chronic wounds. Cochrane Database Syst Rev. 2015;6:CD004123.
Tompach PC, Lew D, Stoll JL. Cell response to hyperbaric oxygen treatment. Int J Oral Maxillofac Surg. 1997;26:82–6.
Sander AL, Henrich D, Muth CM, Marzi I, Barker JH, Frank JM. In vivo effect of hyperbaric oxygen on wound angiogenesis and epithelialization. Wound Repair Regen. 2009;17:179–84.
Kaur S, Pawar M, Banerjee N, Garg R. Evaluation of the efficacy of hyperbaric oxygen therapy in the management of chronic nonhealing ulcer and role of periwound transcutaneous oximetry as a predictor of wound healing response: a randomized prospective controlled trial. J Anaesthesiol Clin Pharmacol. 2012;28:70–5.
Feldmeier JJ. Hyperbaric oxygen therapy and delayed radiation injuries (soft tissue and bony necrosis): 2012 update. Undersea Hyperb Med. 2012;39:1121–39.
Yildiz S, Cimsit M, Ilgezdi S, Uzun G, Gumus T, Qyrdedi T, et al. Hyperbaric oxygen therapy used to treat radiation injury: two case reports. Ostomy Wound Manage. 2006;52:14–6. 18, 20.
We are grateful to Prof. M. Kawashima (Genshindo Kawashima Orthopedic Hospital), Prof. M. Shibayama (Komazawa Women’s University), Dr. M. Komiya (Tokyo Medical and Dental University), Dr. A. Hama, and Dr. D. Thakor for their advice and generous support.
Availability of data and materials
ME contributed by studying the case and writing the manuscript. KY, KO, TO, and YK were involved in the patient’s case. AOka supervised the case. AOku, TM, and SM supported the patient’s treatment with hyperbaric oxygen. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Ethics approval and consent to participate