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Case Reports in Pediatrics
Volume 2018, Article ID 7654278, 5 pages
https://doi.org/10.1155/2018/7654278
Case Report

Successful Management of Blue Rubber Bleb Nevus Syndrome (BRBNS) with Sirolimus

1Division of Hematology, Department of Oncology, Montefiore Medical Center, Bronx, NY, USA
2Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA
3Division of Pediatric Hematology/Oncology/BMT, Nationwide Children’s Hospital, Columbus, OH, USA
4Division of Pediatric Hematology/Oncology, Stead Family Department of Pediatrics, University of Iowa Carver College of Medicine, Iowa City, IA, USA

Correspondence should be addressed to Janice M. Staber; ude.awoiu@rebats-ecinaj

Received 14 August 2018; Accepted 17 September 2018; Published 8 October 2018

Academic Editor: Bernhard Resch

Copyright © 2018 Ugochi O. Ogu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Blue rubber bleb nevus syndrome (BRBNS) is a rare disease with vascular malformations in several systems of the body, most commonly the skin and gastrointestinal tract. Bleeding from the gastrointestinal (GI) tract is a major complication, which may lead to chronic iron deficiency anemia and the need for frequent blood transfusions due to ongoing gastrointestinal blood loss. In this case report, we describe a now 19-year-old female with BRBNS who required six blood transfusions per year and after starting sirolimus is symptom- and transfusion-free.

1. Introduction

Vascular anomalies can be divided into two broad categories, according to the International Society for the Study of Vascular Anomalies (ISSVA) system: vascular malformations and vascular neoplasms [1]. Vascular malformations include slow-flow malformations (with venous, capillary and/or lymphatic components) and fast-flow malformations (with arterial components); while vascular neoplasms undergo mitosis and include such lesions as infantile hemangioma, congenital hemangioma, kaposiform hemangioendothelioma, tufted angioma, hemangiopericytoma, and angiosarcoma [2]. Blue rubber bleb nevus syndrome (BRBNS) is primarily considered a slow-flow venous malformation, although there has been a single case report which includes a lymphatic component [3]. BRBNS usually presents in infancy and childhood and rarely in adulthood [3]. Lesions are blue, rubbery, and compressible, and they occur in several organ/systems and most commonly occur within the skin and gastrointestinal (GI) tract [4].

2. Case Description

A Hispanic female initially presented at three years of age with a history of oropharyngeal bleeding since birth and diffuse skin vascular malformations. Upper and lower GI endoscopies revealed multiple vascular anomalies throughout the entire tract. She was subsequently diagnosed with blue rubber bleb nevus syndrome based on clinical and endoscopic findings. Due to GI bleeding, chronic iron deficiency anemia, and the increased need for blood transfusions, she underwent surgical removal of multiple blebs from her stomach, small intestine, and colon. In addition, she underwent a right colectomy, gastrostomy for tube feedings, and a tracheostomy due to multiple tracheal lesions. At the age of 6.5 years, she was referred to pediatric hematology for the management of anemia. She had long-standing iron deficiency anemia due to significant blood loss from GI bleeding, despite previous RBC transfusions, and intravenous iron therapy. To help control bleeding, she underwent frequent sclerosing therapies to multiple lesions, including the pericervical lesions. An oral aminocaproic acid (Amicar) trial of 10 days duration was not successful to reduce GI bleeding. Despite the above interventions, she remained severely anemic (hemoglobin levels 5.2 gm/dL to 7 gm/dL) and required frequent blood transfusions, as often as every 1–4 months. Due to the significant GI bleeding, her stools were black, tarry, often with bright red blood, occurring 3–4 times a week. At age 15, a trial of daily sirolimus therapy was initiated, based on a case report by Yuksekkaya et al. [4], at a dose of 0.05 mg/kg/dose and levels followed with a target range of 5–10 ng/ml. Within 2 months of initiating sirolimus therapy, she experienced cessation of hematochezia and melena, and her hemoglobin has since remained above 11 g/dl (Figure 1). She is now over 60 months into therapy, remains without anemia, and has not required further blood transfusions. She remains mildly iron deficient to date, most likely due to decreased ability to adequately absorb oral iron due to the blebs and prior GI surgery. No adverse drug reactions have occurred.

Figure 1: Hemoglobin concentration before and after Sirolimus therapy.

3. Discussion

Blue rubber bleb nevus syndrome is a rare congenital disorder with hallmarks of venous malformations on the skin and viscera. The skin and soft tissue lesions rarely cause debilitating disease and are mostly a cosmetic concern [4]. In contrast, the GI lesions are a major cause of morbidity. Patients usually develop severe chronic iron deficiency anemia, requiring multiple transfusions due to persistent GI losses [4].

To date, there is no curative treatment for BRBNS. Management options that have been attempted include iron therapy, blood transfusions, surgical interventions, and pharmacologic agents [4]. Iron therapy and blood transfusions have been employed to alleviate anemia from GI losses. Surgery has been used to eradicate blebs from the skin, soft tissue, or GI tract; however, the blebs eventually recur. Other modalities including laser photocoagulation and sclerotherapy have been applied with limited success. Pharmaceutical agents such as propranolol, octreotide, corticosteroids, interferon alpha, thalidomide, antifibrinolytics, and most recently sirolimus have also been utilized. These have been used based on extrapolation of their efficacy in infantile hemangiomas and other vascular anomalies.

Sirolimus is an immunosuppressant drug that has both antiangiogenic and antineoplastic properties. Its mechanism of action is via pathway inhibition of the mammalian target of rapamycin (mTOR), a serine/threonine kinase regulated by phosphoinositide-3-kinase (PI3K) [5]. It has been used successfully in the management of several vascular anomalies such as kaposiform hemangioendothelioma, tufted angioma, and lymphatic malformations [1]. The first case report describing response of BRBNS to sirolimus was published in 2012 by Yussekkaya et al. [4]. Following that there have been several other reports also describing response to sirolimus [3, 614]. Table 1 details the various reports in the literature so far that have described the use of sirolimus for BRBNS.

Table 1: Articles on BRBNS with Sirolimus therapy.

The exact mechanism of action of sirolimus in BRBNS remains unclear, but proposed mechanisms of action include inhibition of ligand-binding-induced signaling through VEGFR-3 (vascular endothelial growth factor receptor-3) on lymphatic endothelial surface, which would normally result in activation of the PI3K/Akt/mTOR pathway [3, 5]. In addition, c-kit (stem cell growth factor receptor) expression from small venous vessels has been described [15] and has been proposed as a possible mechanism of action, given that c-kit is a tyrosine kinase upstream of mTOR [3].

There exists a dilemma as to what constitutes appropriate duration of therapy. Our patient continues on sirolimus at a dose of 1.2 mg/day (0.024 mg/kg/dose), with target trough level of 2–4 ng/mL and has not experienced any side effects. Her hemoglobin and symptoms remained controlled. Of note, when sirolimus was held for a surgical procedure due to concerns for postsurgical wound healing, her GI bleeding returned within 3 days of discontinuation. Further studies are needed to determine if sirolimus can be safely discontinued, without disease relapse.

In conclusion, sirolimus may be used in management of patients with BRBNS. Our case report describes resolution of GI bleeding and obviation of the need for multiple blood transfusions following initiation of sirolimus therapy. We propose this as an alternative therapy for the treatment of symptomatic BRBNS, especially when other conventional therapies have proved to be unsuccessful.

Abbreviations

BRBNS:blue rubber bleb nevus syndrome
GI:gastrointestinal
mTOR:mammalian target of rapamycin
ISSVA:International Society for the Study of Vascular Anomalies
PI3K:phosphoinositide-3-kinase.

Disclosure

The abstract was presented as a poster at the 2015 ASPHO (American Society of Pediatric Hematology/Oncology) meeting.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  1. J. F. Margolin, H. M. Soni, and S. Pimpalwar, “Medical therapy for pediatric vascular anomalies,” Seminars in Plastic Surgery, vol. 28, no. 2, pp. 79–86, 2014. View at Publisher · View at Google Scholar · View at Scopus
  2. R. Kollipara, L. Dinneen, K. E. Rentas et al., “Current classification and terminology of pediatric vascular anomalies,” American Journal of Roentgenology, vol. 201, no. 5, pp. 1124–1135, 2013. View at Publisher · View at Google Scholar · View at Scopus
  3. R. Salloum, C. E. Fox, C. R. Alvarez-Allende et al., “Response of blue rubber bleb nevus syndrome to sirolimus treatment,” Pediatric Blood and Cancer, vol. 63, no. 11, pp. 1911–1914, 2016. View at Publisher · View at Google Scholar · View at Scopus
  4. H. Yuksekkaya, O. Ozbek, M. Keser, and H. Toy, “Blue rubber bleb nevus syndrome: successful treatment with sirolimus,” Pediatrics, vol. 129, no. 4, pp. e1080–e1084, 2012. View at Publisher · View at Google Scholar · View at Scopus
  5. A. M. Hammill, M. Wentzel, A. Gupta et al., “Sirolimus for the treatment of complicated vascular anomalies in children,” Pediatric Blood and Cancer, vol. 57, no. 6, pp. 1018–1024, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. A. Taddio, E. Benelli, C. Pierobon, S. Martelossi, I. Berti, and A. Ventura, “From skin to gut,” Journal of Pediatrics, vol. 163, no. 2, p. 610, 2013. View at Publisher · View at Google Scholar · View at Scopus
  7. B. Warner, A. Butt, and S. Cairns, “Sirolimus is a successful treatment for recurrent iron deficiency anaemia in blue rubber bleb naevus syndrome,” Journal of Pediatric Gastroenterology and Nutrition, vol. 61, no. 5, p. e24, 2015. View at Publisher · View at Google Scholar · View at Scopus
  8. L. Ferrés-Ramis, N. Knöpfel, J. Salinas-Sanz, and A. Martín-Santiago, “Rapamycin in the Treatment of Blue Rubber Bleb Nevus Syndrome,” Actas Dermo-Sifiliográficas (English Edition), vol. 106, no. 2, pp. 137-138, 2015. View at Publisher · View at Google Scholar · View at Scopus
  9. B. Ozgonenel and A. Martin, “Low-dose sirolimus controls recurrent iron deficiency in a patient with blue rubber bleb nevus syndrome,” Pediatric Blood and Cancer, vol. 62, no. 11, pp. 2054-2055, 2015. View at Publisher · View at Google Scholar · View at Scopus
  10. H. Cardoso, J. A. Dias, M. Silva et al., “Gastrointestinal: successful treatment with sirolimus of a patient with blue rubber bleb nevus syndrome,” Journal of Gastroenterology and Hepatology, vol. 31, no. 3, p. 519, 2016. View at Publisher · View at Google Scholar · View at Scopus
  11. A. Ünlüsoy Aksu, S. Sari, Ö. E. Gürkan, and B. Dalgiç, “Favorable response to sirolimus in a child with blue rubber bleb nevus syndrome in the gastrointestinal tract,” Journal of Pediatric Hematology/Oncology, vol. 39, no. 2, pp. 147–149, 2017. View at Publisher · View at Google Scholar · View at Scopus
  12. C. Akyuz, H. Susam-Sen, and B. Aydin, “Blue rubber bleb nevus syndrome: promising response to sirolimus,” Indian Pediatrics, vol. 54, no. 1, pp. 53-54, 2017. View at Publisher · View at Google Scholar · View at Scopus
  13. K. L. Wang, S. F. Ma, L. Y. Pang et al., “Sirolimus alternative to blood transfusion as a life saver in blue rubber bleb nevus syndrome: a case report,” Medicine (Baltimore), vol. 97, no. 8, Article ID e9453, 2018. View at Publisher · View at Google Scholar · View at Scopus
  14. H. Kizilocak, G. Dikme, and T. Celkan, “Sirolimus experience in blue rubber bleb nevus syndrome,” Journal of Pediatric Hematology/Oncology, vol. 40, no. 2, pp. 168-169, 2018. View at Publisher · View at Google Scholar · View at Scopus
  15. C. Mogler, C. Beck, A. Kulozik, R. Penzel, P. Schirmacher, and K. Breuhahn, “Elevated expression of c-kit in small venous malformations of blue rubber bleb nevus syndrome,” Rare Tumors, vol. 2, no. 2, pp. 99-100, 2010. View at Publisher · View at Google Scholar