Journals / Respiratory Case Reports / 2021 / Cilt: 10 - Sayı: 3

Hemangiolymphangioma with Accompanying Interstitial Lung Disease: A Rare Case

İnterstistiyel Akciğer Hastalığı ile Seyreden Hemanjiyolenfanjioma: Nadir Bir Olgu

Pages
180–185
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

After the VATS procedure, the patient developed chylotho- rax, and the pathology results indicated hemangio- lymphangioma.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Vascular anomalies are pathologies that occur in embryonic life that affect the lymphatic and capillary systems, and can be classified as vascular tumors or vascular malformations, according to their histologi- cal features.
📊
Key Findings & Data:Hemangiolymphangiomas are benign vascular tumors containing lymphatic and capillary-system elements with a reported incidence of 1: 12,000 in newborns.
💡
Conclusion & Impact:After the VATS procedure, the patient developed chylotho- rax, and the pathology results indicated hemangio- lymphangioma.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Vascular anomalies are pathologies that occur in embryonic life that affect the lymphatic and capillary systems, and can be classified as vascular tumors or vascular malformations, according to their histologi- cal features. They are rare and are mostly detected in the first years of life. Hemangiolymphangiomas are benign vascular tumors containing lymphatic and capillary-system elements with a reported incidence of 1: 12,000 in newborns. The cases reported to date have been in the head (oral cavity, orbita, etc.), neck and mediastinum regions. We presented here a case of a 17-year-old male patient who was diag- nosed with hemangiolymphangioma after a video- assisted lung biopsy (VATS) with accompanying inter- stitial lung disease. The patient, who had no history of chronic disease, presented to the outpatient clinic complaining of cough and shortness of breath for eight months. Interstitial lung features were observed in the patient’s thorax computer tomography. After the VATS procedure, the patient developed chylotho- rax, and the pathology results indicated hemangio- lymphangioma.

Özet

Vasküler anomaliler, embriyonik yaşamda oluşan, lenfatik ve kapiller sistemleri etkileyen patolojilerdir ve histolojik özelliklerine göre vasküler tümörler veya vasküler malformasyonlar olarak sınıflandırılırlar. Nadir görülürler ve daha çok yaşamın ilk yıllarında saptanırlar. Hemanjiyolenfanjiyomlar da lenfatik ve kapiller sistem elemanları içeren, benign bir vasküler tümördür. İnsidansı yenidoğanlarda 1/12.000 olarak bildirilmiştir. Bugüne dek bildirilen olgular baş bölgesi (ağız boşluğu, orbita vs), boyun ve mediasten bölge- lerindedir. Biz de bu makalede interstistiyel akciğer hastalığı ile seyreden ve yapılan tanısal video yardımlı akciğer biyopsisi (VATS) işlemi sonrasında hemanjiyo- lenfanjiyoma tanısı alan 17 yaşında bir erkek hastayı sunduk. Kronik bir hastalığı olmayan ve sekiz aydır olan öksürük ve nefes darlığı ile polikliniğe başvuran hastaya çekilen toraks tomografisinde interstistiyel akciğer özellikleri görülmüş olup; VATS işlemi sonra- sında hastada şilotoraks gelişti. Patoloji sonucu he- manjiyolenfanjiyom olarak sonuçlandı.

🔖

Cite This Article

Metin, M., Seyhan, E. C., Fener, N., Oğuztürk, G., Mahmuti, S. O., Demirkol, E. Y., Çetınkaya, E. (2022). Hemangiolymphangioma with Accompanying Interstitial Lung Disease: A Rare Case. Respiratory Case Reports, Cilt: 10 - Sayı: 3, 180–185. https://ajindex.com/articles/588876

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (6)

  1. Manickam S, Sasikumar P, Kishore BN, and Joy S. He- mangiolymphangioma of buccal mucosa: A rare case report. J Oral Maxillofac Pathol 2017
  2. 21(2): 282-285. [CrossRef] 2. Schwartz RA, Mancini M, Lin RL. Arterial Vascular Mal- formations Including Hemangiomas and Lymphangiomas Clinical Presentation. Medscape Education Global. Ac- cess date: 16 March 2021. Place of access: https://emedicine.medscape.com/article/1018071- clinical. 3. Kadakia KC, Patel SM, Yi ES, Limper AH. Diffuse pulmo- nary lymphangiomatosis. Can Respir J 2013
  3. 20(1):52- 54. [CrossRef] 4. Martínez-Bucio V, De la Puente-Murgía R, Gallardo- Meza A, Zapata-Martínez SG, Zertuche-Coindreau JM, López-Valdés JC. Pulmonary haemangiolymphangioma as cause of hemodynamic decompensation, Revista Médica del Hospital General de México, Volume 79, Is- sue 4, 2016, Pages 210-215, ISSN 0185-1063. [CrossRef] 5. Mulliken JB, Glowacki J. Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg 1982
  4. [CrossRef] 6. Faul JL, Berry GJ, Colby TV, Ruoss SJ, Walter MB, Rosen GD, Raffin TA. Thoracic Lymphangiomas, Lymphangiec- tasis, Lymphangiomatosis, and Lymphatic Dysplasia Syn- drome. April 2000. American journal of respiratory and critical care medicine. 161. 1037-46. [CrossRef] 7. Nakamura T, Tamanuki K, Ko, G, Oguri, M, Akita C, Kitaoka C, Nakamura T and Saikawa, Y. Chronic throm- boembolic pulmonary hypertension related to hemangio- lymphangioma. Case Reports in Clinical Medicine 2014
  5. [CrossRef] 8. Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management, J Surg Case Rep 2017
  6. 2017(8):rjx168. [CrossRef]