Renal myxoma - a case report of a rare kidney tumor, its differential diagnosis and literature review

被引:2
|
作者
Hudairy, Rawan [1 ]
Buksh, Omar [2 ]
Akram, Rabea [2 ]
Alammari, Adel [2 ]
Al-Maghrabi, Jaudah [1 ]
Almansouri, Zuhoor [1 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Pathol, Jeddah, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Urol, Jeddah, Saudi Arabia
关键词
Rare; Renal tumor; Myxoma;
D O I
10.1002/iju5.12439
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Myxoma is a rare benign kidney tumor. Only 18 cases have been described in the literature. We report a new case of renal myxoma that arises from the renal parenchyma. Case presentation: A 56-year-old man, medically free, presented complaining of intermittent vague left-side abdominal pain for 1year, otherwise no history of gross hematuria or lower urinary tract symptoms. Clinical examination revealed a soft, non-tender abdomen. All laboratory investigations were within normal. Abdominal and pelvic computed tomography scan with contrast revealed a large mass located in the upper pole of left kidney with the possibility of renal cell carcinoma. A laparoscopic-assisted left robotic radical nephrectomy was performed. Microscopic examination revealed renal myxoma. Conclusion: Renal myxoma is a very rare benign kidney tumor with excellent prognosis. Considering its rarity, it is important to recognize this entity to avoid diagnostic errors with other neoplasms with prominent myxoid features.
引用
收藏
页码:207 / 210
页数:4
相关论文
共 50 条
  • [41] Odontogenic myxoma of the anterior mandible: Case report of a rare entity and review of the literature
    Sohrabi, Maryam
    Dastgir, Ramtin
    CLINICAL CASE REPORTS, 2021, 9 (08):
  • [42] PRIMARY CARCINOID OF THE KIDNEY - DIFFERENTIAL-DIAGNOSIS FOR RENAL-CELL CARCINOMA - CASE-REPORT AND REVIEW OF LITERATURE
    STEIN, R
    STEINBACH, F
    MULLER, SC
    STORKEL, S
    HOHENFELLNER, R
    AKTUELLE UROLOGIE, 1992, 23 (04) : 183 - 185
  • [43] Rare presentation of an atrial myxoma in an adolescent patient: a case report and literature review
    Macias, Eduardo
    Nieman, Elizabeth
    Yomogida, Kentaro
    Petrucci, Orlando
    Javidan, Cylen
    Baszis, Kevin
    Anwar, Shafkat
    BMC PEDIATRICS, 2018, 18
  • [44] Rare presentation of an atrial myxoma in an adolescent patient: a case report and literature review
    Eduardo Macias
    Elizabeth Nieman
    Kentaro Yomogida
    Orlando Petrucci
    Cylen Javidan
    Kevin Baszis
    Shafkat Anwar
    BMC Pediatrics, 18
  • [45] Conjunctival myxoma – atypical presentation of a rare tumour: case report and review of literature
    Neharika Sharma
    Stephen O’Hagan
    Gael Phillips
    BMC Ophthalmology, 16
  • [46] Malignant Gastrointestinal Neuroectodermal Tumor: A Case Report and Literary Review for a Rare Differential Diagnosis
    Baccaro, Cinzia
    Zorzetti, Noemi
    Cuoghi, Manuela
    Fornelli, Adele
    Franceschini, Tania
    Coluccelli, Sara
    Cennamo, Vincenzo
    Navarra, Giuseppe Giovanni
    SURGERIES, 2023, 4 (02): : 235 - 245
  • [47] Renal myelolipoma: A rare extra-adrenal tumor in a rare site: A case report and review of the literature
    Ghaouti M.
    Znati K.
    Jahid A.
    Zouaidia F.
    Bernoussi Z.
    Mahassini N.
    Journal of Medical Case Reports, 7 (1)
  • [48] Isolated Renal Metastasis from Neuroendocrine Tumor: How Rare is Rare? A Case Report and Review of the Literature
    Ali, Mohga
    Lengu, Irma
    Ganesan, Santhi
    JOURNAL OF UROLOGICAL SURGERY, 2016, 3 (01): : 25 - 27
  • [49] Glomus Tumor of the Kidney: Case Report and Literature Review
    Sasaki, Kotaro
    Bastacky, Sheldon I.
    Hrebinko, Ronald L.
    Parwani, Anil V.
    Zynger, Debra L.
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2011, 19 (03) : 393 - 397
  • [50] Heavily Pigmented Renal Cell Carcinoma: A Case Report, With Review of the Literature and Differential Diagnosis
    Rossi, Giulio
    Cadioli, Annamaria
    Costantini, Matteo
    Del Buono, Maria Grazia
    Oleari, Giorgio
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2009, 17 (02) : 167 - 169