CEREBRAL SALT WASTING SYNDROME IN A PATIENT WITH PRIMARY CNS LYMPHOMA

被引:4
|
作者
Prochazka, Vit [1 ]
Kubova, Zuzana [1 ]
Raida, Ludek [1 ]
Papajik, Tomas [1 ]
Paucek, Boris [2 ]
Indrak, Karel [1 ]
机构
[1] Univ Hosp, Dept Hematooncol, Olomouc 77520, Czech Republic
[2] Medihope Magnet Imaging Ctr, Prostejov, Czech Republic
来源
BIOMEDICAL PAPERS-OLOMOUC | 2009年 / 153卷 / 03期
关键词
Cerebral salt wasting; Lymphoma; Hyponatremia; HYPONATREMIA;
D O I
10.5507/bp.2009.037
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: In patients with severe central nervous system (CNS) diseases, life-threatening hyponatremia results from two main causes: the syndromes of inappropriate secretion of antidiuretic hormone (SIADH) and cerebral salt wasting (CSW). Clinical manifestations of the two conditions may be similar but their pathogeneses are fundamentally diverse. Distinguishing SIADH from CSW is based on the differential diagnoses of dilutional hyponatremia due to an excessive amount of water in the body (SIADH) and depletional hyponatremia caused by extensive natriuresis (CSW). Methods and Results: We report the case of a 48-year-old, previously healthy male with a diffuse large B-cell lymphoma affecting the area of the basal ganglia and the right part of the thalamus and oppressing the third brain ventricle. After admission to the Department of Hemato-oncology, the patient was soporous and laboratory tests revealed severe serum hyponatremia, hypochloremia, hypoosmolality and marked polyuria with normal serum levels of urea, creatinine, glucose and calcium. Urinalysis showed high specific gravity of the urine and extreme wasting of sodium, chloride and kalium ions. Overall fluid balance was negative. After the first chemotherapy cycle, the CT scan confirmed regression of the tumour site. This was accompanied by patient's improved cognition as well as decreased polyuria and urine electrolyte excretion. Eventually, it was concluded that the diagnosis was cerebral salt wasting syndrome. Conclusion: We noted a so far unpublished case of a 48-year-old male with the diagnosis of primary CNS lymphoma (DLBCL) affecting deep structures of the brain and associated with CSW.
引用
收藏
页码:219 / 220
页数:2
相关论文
共 50 条
  • [21] CEREBRAL SALE WASTING SYNDROME OR SIADH: HYPONATREMLA IN A PATIENT WITH METASTATIC BRAUN LYMPHOMA
    Afsharimani, SeyedAmirhossein
    Dowlatshahi, Samaneh
    Friedman, Harvey
    JOURNAL OF GENERAL INTERNAL MEDICINE, 2014, 29 : S331 - S331
  • [22] WHAT IS THE DIAGNOSIS - CEREBRAL SALT WASTING SYNDROME
    DEDEOGLU, IO
    MATANGUIHAN, ET
    SPRINGATE, JE
    PEDIATRIC NEPHROLOGY, 1995, 9 (03) : 395 - 396
  • [23] An Integrative Review of Cerebral Salt Wasting Syndrome
    Oh, HyunSoo
    Seo, WhaSook
    JOURNAL OF NEUROSCIENCE NURSING, 2020, 52 (06) : 289 - 294
  • [24] Cerebral salt wasting syndrome in a child with SSPE
    Calik, Mustafa
    Iscan, Akin
    Abuhandan, Mahmut
    Geter, Suleyman
    Atas, Ali
    Kati, Mahmut
    Cece, Hasan
    JOURNAL OF PEDIATRIC NEUROLOGY, 2012, 10 (03) : 221 - 224
  • [25] Cerebral salt wasting syndrome: A review - Comments
    Weir, BKA
    NEUROSURGERY, 1996, 38 (01) : 160 - 160
  • [26] Cerebral salt wasting syndrome in bacterial meningitis
    Attout, H.
    Guez, S.
    Series, C.
    ANNALES D ENDOCRINOLOGIE, 2007, 68 (05) : 395 - 397
  • [27] Cerebral salt wasting syndrome in tuberculous meningitis
    Jabbar, Abdul
    Farrukh, Syed Nadir
    Khan, Rabbia
    JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, 2010, 60 (11) : 964 - 965
  • [28] Cerebral salt wasting syndrome or secondary hypoadrenalism?
    Dickstein, G
    ISRAEL MEDICAL ASSOCIATION JOURNAL, 2001, 3 (06): : 469 - 470
  • [29] Does cerebral salt wasting syndrome exist?
    Leblanc, P. -E.
    Cheisson, G.
    Geeraerts, T.
    Tazarourte, K.
    Duranteau, J.
    Vigue, B.
    ANNALES FRANCAISES D ANESTHESIE ET DE REANIMATION, 2007, 26 (11): : 948 - 953
  • [30] Distinguishing cerebral salt wasting syndrome and syndrome of inappropriate ADH in a patient with traumatic brain injury
    Mohamed, Hassan
    Shorten, George
    BMJ CASE REPORTS, 2021, 14 (03)