1. Introduction
The Republic of the Congo is the sixth oil producing country in Africa south of SAHARA [1]. As a result, exposure to inhalation of hydrocarbons by air pollution is reported by populations, although exposure to hydrocarbons is a factor harmful to health [2]. A meta-analysis published in 2000 of 14 case-control studies devoted to chronic glomerulopathies does not show a causal role (initiator) of organic solvents but suggests an acceleration of the evolution towards the IRT when the pathology is installed: thus, the occupational exposure to solvents appears likely to worsen the nephropathy of hypertensives and diabetics [3]. Exposure to organic (hydrocarbons) solvents has been shown to double the risk of IgA glomerulonephritis and quadruple the risk of extra membranous glomerulonephritis (GEM) [4] [5] [6]. Thus we report a case of chronic glomerulonephritis after exposure to hydrocarbons. This patient from Pointe Noire city is an isolated case in Congolese nephrology practice, although several cases have been reported in the literature [2].
2. Observation
He is a 39-year-old patient working for 5 years as a hydrocarbon transporter, having a high exposure to hydrocarbons, more than 2 hours per week. He had no history of herbal medicine, no edema, no diabetes, no high blood pressure, and he had no infectious diseases and there was no notion of kidney disease in the family.
He was hospitalized for generalized apyretic convulsions with impaired renal function.
On clinical examination after stabilization of the patient with diazepam 10 mg half ampoule intramuscularly, we have:
Discreet edema of the lower limbs keeping the cup with puffiness of the face hyposthenuria, with the urine strip (US):
Proteinuria and hematuria were positive at one to one cross (+), a PH at 6. On the other hand the urinary cylinders, glycosuria, leukocyturia and nitrites were negative.
Blood pressure at 170/110 mmhg or hypertension. The respiratory rate is 20 cycles per minute which is normal.
In biology we have:
The albuminuria to creatininuria ratio at 300 mg/g (ACR) is glomerular involvement. The creatinine level at entry was 195 mg/l, i.e. a clearance of 3 ml/Min/1.72 m2 according to CKD-EPI.
Entrance blood urea was 3.57 g/l; Calcemia at 63 mg/l; AgHbs: negative; Anti HCV AC: negative; syphilitic serology was negative; the cholesterol/HDL ratio at 4.2 with standards < 5; the LDL-Cholesterol/HDL Cholesterol ratio at 2.9 is normal with standard < 3.5; the HbA1 at 4.8% is normal with standard between 4% to 6%; fasting blood sugar was 1.01 g/l.
And the hemogram showed: Hb at 7.7 g/dl, VGM = 91 (Normal) and CCMH = 29.1 (normal) or Normochromic Normocytic anemia
HIV retroviral serology has been negative.
The abdominopelvic ultrasound revealed normal size, dedifferentiated kidneys.
The patient received 7 sessions of hemodialysis with a right femoral catheter with heparin.
The evolution is marked afterwards by the disappearance of edema and a satisfactory blood pressure balance and a drop in urea to 1 g/l and the creatinine level to 23 mg/l, i.e. a clearance of 40 ml/Min/1.73 m2 according to CKD-EPI. The patient was enrolled in chronic hemodialysis.
3. Discussion
A meta-analysis published in 2000 of 14 case-control studies devoted to chronic glomerulopathies does not show a causal role for solvents but suggests an acceleration of the evolution towards IRCT when the pathology is installed: thus, the solvents appear susceptible to aggravate the nephropathy of hypertensives and diabetics [3].
In a French case-control study published in 2007, the risk of progression from Berger disease to the IRCT is doubled in the event of high exposure to solvents [4]. Exposure to organic solvents affects the functioning of the kidneys, this has been a hypothesis since 2007 issued by the American Society of Nephrology [2] [3].
In fact, the GN-PROGRESS study described that exposure to organic solvents gave chronic glomerulonephritis and accelerated the onset of end-stage renal disease. Exposure to organic (hydrocarbons) solvents has been shown to double the risk of IgA glomerulonephritis and quadruple the risk of extra membranous glomerulonephritis (GEM) [4] [5] [6].
In our case, the patient was exposed to hydrocarbons for 5 years with a high exposure either more than 2 hours per day or a high exposure and he was immunocompetent. What is found in the GN PROGRESS study.
The Renal Biopsy Puncture (PBR) was not done in our case so histologically we do not know the lesion; however the lesions of GEM, HSF and IgA have been described by several authors [4] - [14]. Hence the importance of establishing the histology of lesions of chronic renal hydrocarbon disease in our environment.
The patient has chronic glomerulonephritis with tubulointerstitial involvement due to the presence of hyposthenuria. This is identical to the observation of Yaqoob M et al. [7] who, after post exposure to hydrocarbons, found chronic glomerulonephritis with tubular involvement. This could be explained by the deposits of intra-tubular hydrocarbons. FANCONI syndromes have even been described in the event of exposure to hydrocarbons [15] [16] [17] [18].
4. Conclusion
Congo Brazzaville is an oil producing country; we have many people exposed to hydrocarbons. Apart from this case, we must do early screenings among personnel exposed to hydrocarbons. This study should consist of performing urine test strips, 24-hour proteinuria or albuminuria and creatininemia to have the Albumin Creatinine Ratio, Red Cell-Leukocyte Minutes flow rate, creatininemia and blood urea. Renal or even abdominopelvic ultrasound and Renal Biopsy Puncture are not systematic in the detection and monitoring of renal diseases in subjects exposed to hydrocarbons. But the biopsy is important to establish what histological lesions are found. We must work with specialists in occupational medicine because this injury could be considered as an occupational disease.
Informed Consent
Patient consent has been obtained.
Thanks
Professor Malick Faye
Doctor Noé Motoula
Professor Saraladevi Naicker
Professor Boucar Diouf
Abbreviations
BU: Urinary strip.
ACR: Albumin Creatinin Ratio.
HbA1C: Glycated Hemoglobin.
HLM: Red blood cell-minute leukocyte throughput.
PBR: Renal Biopsy Puncture.
CKD-EPI: Chronic Kidney Disease Epidemiology.