Journals / Gazi Medical Journal / 2018 / Cilt: 29 - Sayı: 1

Cystic Lymphangioma: A Rare Disease of the Adrenal Gland

Kistik lenfanjioma: Adrenal Bezin Nadir Bir Hastalığı

Pages
67–68
Publication Date
2022-10-19
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)

However, histopathology reported as a rare adrenal cysticlymphangioma.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Cystic adrenal neoplasms are uncommon and may be discovered incidentally ormay be symptomatic but cystic lymphangioma is a rare benign tumour.
📊
Key Findings & Data:Thetumour usually occurs in the neck or axilla and rarely involves the adrenal gland.Here we report a case of a 42-year-old lady presented with symptoms ofanorexia, vomiting and lethargy for 3 weeks.
💡
Conclusion & Impact:However, histopathology reported as a rare adrenal cysticlymphangioma.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Cystic adrenal neoplasms are uncommon and may be discovered incidentally ormay be symptomatic but cystic lymphangioma is a rare benign tumour. Thetumour usually occurs in the neck or axilla and rarely involves the adrenal gland.Here we report a case of a 42-year-old lady presented with symptoms ofanorexia, vomiting and lethargy for 3 weeks. Apart from evidence of milddehydration, there was no positive physical examination. Upon admission, herblood urea and creatinine was high and she was diagnosed with end stage renaldisease secondary to chronic glomerulonephritis. Ultrasound of the abdomenrevealed an incidental right adrenal mass and computed tomography (CT) scanshowed a lesion with Hounsfield unit (HU) of 13, 20 and 21 on plain, venous anddelayed phase, giving an absolute wash out of 12.5%. Biochemical tests wereconsistent with a non-functioning adrenal incidentaloma. Hence she wassubjected for right retroperitoneoscopic adrenalectomy in view of suspicious ofadrenal malignancy. However, histopathology reported as a rare adrenal cysticlymphangioma.

Özet

Kistik adrenal neoplaziler seyrektir ve tesadüfen bulunabilir veya semptomatik olabilirler, ancak kistik lenfanjiom nadir görülen benign bir tümördür. Tümör genellikle boyun veya aksillada görülür ve nadiren adrenal bezi tutar. Bu olguda, 3 haftadır anoreksi, kusma ve letarji belirtileri gösteren 42 yaşındaki kadın vakayı sunuyoruz. Hafif dehidratasyon dışında, herhangi bir pozitif fizik muayene bulgusu saptanmadı. Yatış sonrası, kan üre ve kreatinin değerleri yüksekti ve kronik glomerülonefrite sekonder son dönem böbrek hastalığı tanısı aldı. Karın ultrasonunda tesadüfen sağ adrenal kitle ve bilgisayarlı tomografide (CT) ise düz, venöz ve gecikmiş fazda Hounsfield ünitesi (HU) 13, 20 ve 21 olan bir lezyon gösterdi ve % 12.5'lik mutlak yıkanma sağladı. Biyokimyasal testler, fonksiyonel olmayan adrenal insidentaloma ile uyumlu idi. Bu nedenle, adrenal malignite şüphesi nedeniyle sağ retroperitoneoskopik adrenalektomi yapıldı. Bununla birlikte histopatoloji ender görülen adrenal kistik lenfanjiom olarak rapor edilmiştir.

🔖

Cite This Article

OTHMAN, S., RASHİD, N. F. A., SUHAİMİ, S. N. A., MUHAMMAD, R., WAHAB, N. A. (2022). Cystic Lymphangioma: A Rare Disease of the Adrenal Gland. Gazi Medical Journal, Cilt: 29 - Sayı: 1, 67–68. https://ajindex.com/articles/519804

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (4)

  1. Erickson LA, Lloyd RV, Hartman R, Thompson G. Cystic adrenal neoplasms. Cancer. 2004;101(7):1537-44.
  2. Joliat GR, Melloul E, Djafarrian R, Schmidt S, Fontanella S, Yan P, Demartines N, Halkic N. Cystic lymphangioma of the adrenal gland: report of a case and review of the literature. World journal of surgical oncology. 2015;13:58. Van Oudheusden TR, Nienhuijs SW, Demeyere TB, Luyer MD, de Hingh IH. Giant cystic lymphangioma originating from the lesser curvature of the stomach. World journal of gastrointestinal surgery. 2013;5:264. Ellis CL, Banerjee P, Carney E et al. Adrenal lymphangioma: clinicopathologic and immunohistochemical characteristics of a rare lesion. Hum Pathol. 2011; 42: 1013-8
  3. Ates LE, Kapran Y, Erbil Y et al. Cystic lymphangioma of the right adrenal gland. Pathol Oncol Res. 2005; 11: 242-4
  4. Zhao M, Gu Q, Li C, Yu J, Qi H. Cystic lymphangioma of adrenal gland: a clinicopathological study of 3 cases and review of literature. International journal of clinical and experimental pathology. 2014;7:5051. Faten Hadjkacem, Mouna Ammar, Ayman Maalej et al. Cystic lymphangioma of the adrenal gland: A case report and a review of the literature. American Journal of Medicine Studies. 2015; 3: 1-3 Poncelet V. Retroperitoneal cystic lymphangioma. Journal Belge Radiol. 1998. 81:245 Geramizadeh B, Yazdanpanah S, Salahi H, Marzban M. Adrenal Cystic Lymphangioma Presented With Hypertension: A Case Report. Nephro-urology monthly. 2015;7::e27049. Liu B, Li Y, Wang S. Adrenal lymphangioma removed by a retroperitoneoscopic procedure. Oncol Lett. 2013;5:539–40