SN Vs SNA

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Sindrom Nefrotik

Sindrom Nefritik Akut


Nyimas Annissa MA, dr.

SINDROMA NEFROTiK (SN)

PRIMARY

Minimal Change Nephropathy


Focal Glomerulosclerosis
Membranous Nephropathy
Hereditary

Etiology SN

SECONDARY

DM
SLE
Viral Infection
Preeclampsia

Anak2/dewasa
Wajah bengkak
Bengkak di seluruh tubuh
Kencing berbusa
Kencing keruh
Kencing berdarah

ANAMNESIS

Pitting edema
Edema anasarka
Asites
Efusi pleura
Hipertensi

Pemeriksaan fisik

Darah rutin
Urin rutin : proteinuria +3 (3 gram/L), eritrosit (+), Bence Jones protein (+)
oval fat bodies (+)
Profil lipid : LDL HDL TG Kol Tot
Albumin serum
Albumin Urin
Elektrolit
Biopsi renal

Pemeriksaan penunjang

Oval fat bodies urine

Minimal change disease (MCD): is the most common cause of nephrotic syndrome in children. It owes its
name to the fact that the nephrons appear normal when viewed with an optical microscope as the lesions are
only visible using an electron microscope. Another symptom is a pronounced proteinuria.
Focal segmental glomerulosclerosis (FSGS): is the most common cause of nephrotic syndrome in adults.[15] It
is characterized by the appearance of tissue scarring in the glomeruli. The term focal is used as some of the
glomeruli have scars, while others appear intact; the term segmental refers to the fact that only part of the
glomerulus suffers the damage.
Membranous glomerulonephritis (IMN): The inflammation of the glomerular membrane causes increased
leaking in the kidney. It is not clear why this condition develops in most people, although an auto-immune
mechanism is suspected.[15]
Membranoproliferative glomerulonephritis (MPGN): is the inflammation of the glomeruli along with the
deposit of antibodies in their membranes, which makes filtration difficult.
Rapidly progressive glomerulonephritis (RPGN): (Usually presents as a nephritic syndrome) A patients
glomeruli are present in a crescent moon shape. It is characterized clinically by a rapid decrease in the
glomerular filtration rate (GFR) by at least 50% over a short period, usually from a few days to 3 months. [16]

Histology

MINIMAL
CHANGE
DISEASE
(MCD)

Focal segmental
glomerulosclerosis
(FSGS):

Glomerulus terluka
Sifatnya sclerosis
Hanya beberapa segmental
Paling banyak dewasa

Membranous
glomerulonephritis
(IMN):
Inflamasi di membran glmerulus
Dinding kapiler menebal

Membranoproliferativ
e glomerulonephritis
(MPGN):
Inflamasi glomerulus
Deposit antibody

Rapidly progressive
glomerulonephritis
(RPGN):

Glomerulus berbentuk
cressent moon shape)
GFR turun drastis

SNA
Gagal Ginjal
Gagal Jantung
Diabetic Nephropathy

DD

Penegakkan diagnosis

Prednisone (40mg/day) sediaan 5mg tappering dose


Cyclophospamide (2-3 mg/kg/day) sediaan IV 500mg 12 minggu
Cyclosporine (5-6 mg/kg/day) sediaan IV 50 mg
Rituximab (375 mg/m2) sediaan IV 10mg/ml
Furosemide (1 mg/kgbb/day)
Spironolakton (2mg/kgbb/day)
Albumin (1 gram/kgbb/day)
Captopril

Tatalaksana

REMISI

RELAPS
RELAPS
JARANG
RELAPS SERING
DEPENDEN
STEROID

proteinuria negatif atau trace (proteinuria < 4 mg/m2 LPB/jam) 3


hari berturut-turut dalam 1 minggu
proteinuria 2+ (proteinuria 40 mg/m2 LPB/jam) 3 hari
berturut-turut dalam 1 minggu 3
relaps terjadi kurang dari 2 kali dalam 6 bulan pertama setelah
respons awal atau kurang dari 4 kali per tahun pengamatan
(frequent relaps) : relaps terjadi 2 kali dalam 6 bulan pertama
setelah respons awal atau 4 kali dalam periode 1 tahun
relaps terjadi pada saat dosis steroid diturunkan atau dalam 14 hari
setelah pengobatan dihentikan, dan hal ini terjadi 2 kali berturutturut
tidak terjadi remisi pada pengobatan prednison dosis penuh (full
dose) 2 mg/kgBB/hari selama 4 minggu.

RemiSION and relaps


RESISTEN
STEROID

Infeksi :

Non Infeksi :

GNAPS
(Glomerulonefritis
Akut Pasca Streptococcus)
Rx Ag Ab
imuncomplex

Vaskulitis
SLE
Cryoglobulinemia
Polyartritis Nodusa
Henoch Scholein purpura
Berger disease

Sindrom nefritis akut

Laki-laki
Usia 2-14 tahun
Awalnya bengkak di mata,
kemudian wajah
BAK berwarna merah kehitaman
BAK sedikit (oliguri)
Demam
malaise

Anamnesis

Nyeri kepala
Mual
Muntah
Nyeri pinggang
Nyeri sendi
Kelainan kulit ?
Riwayat batuk pilek sakit
tenggorokan ??

KU lemah
Hipertensi
Dyspnea
Edema palpebra dan wajah
Mimisan
JVP
Efusi pleura
Rash, pallor, kelainan kulit

Pemeriksaan fisik

Darah rutin
Urin rutin :
- gross hematuri
- proteinuria
- RBC
- WBC
- granullar cast
- oval fat bodies (kronis)

BUN (blood urea nitrogen)


Elektrolit
Pemeriksaan Complement
serum
ASTO (+)
Biopsi renal

Pemeriksan penunjang

Sttary sky imunofluorescence

Inj. Penicilin G 250 mg / 400.000 IU /day


PO. Cephalexin 4 x 250 mg
PO. Eritromicin 4 x 400 mg selama 10 hari
Inj. Furosemide
Inj. Nitroprusside
PO. Nifedipine 1x 5mg

Tatalaksana

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