Limitation of Kidney Biopsy in Detecting Crescentic Lesions in IgA Nephropathy
Author(s) -
Osamu Hotta,
Yoshio Taguma,
Katsuhiko Sudo,
Kohsei Kurosawa
Publication year - 1993
Publication title -
the nephron journals/nephron journals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.951
H-Index - 72
eISSN - 2235-3186
pISSN - 1660-8151
DOI - 10.1159/000187534
Subject(s) - medicine , nephropathy , biopsy , kidney disease , pathology , renal biopsy , nephrology , kidney , endocrinology , diabetes mellitus
Osamu Hotta, MD, Department of Nephrology, Sendai Shakaihoken Hospital, 3-16-1 Tsutsumimachi, Sendai 981 (Japan) Dear Sir, Whether cellular crescentic lesions are present or not is one of the important factors in predicting the prognosis of patients with IgA nephropathy (IgAN) [1], and consequently affects the choice of therapeutic interventions. However, cellular crescents are usually distributed in a focal manner, especially in the milder or early phase of IgAN. Therefore, the accuracy in detecting crescentic lesions may depend to a large extent on the size of the biopsy specimen [2]. In an attempt to clarify the limitation of kidney biopsy in detecting cellular crescentic lesions in IgAN, we investigated the relationship between the size of biopsy specimens and the frequency of the presence of cellular crescentic lesions in 206 subjects with IgAN. Renal biopsy specimens were obtained by surgical (184 cases) or percutaneous (22 cases) needle biopsy. Two specimens were obtained from each patient. About two-thirds of each specimen from the same patient was processed for light microscope (LM) study. The remaining one-third of each specimen was processed for immunofluorescence and electron microscope study. The number of glom-eruli and the presence or absence of cellular crescentic lesions were examined in two sections of each specimen for LM study from the same patient. In addition to the relationship between the incidence of the presence of cellular crescentic lesions and the total number of glomeruli in the biopsy specimen, the relationship between the incidence of cellular crescentic lesions in one of two specimens (the smaller one and the larger one) and the number of glomeruli in the smaller specimen was examined. The incidence of cellular crescentic lesions in one of the two specimens was determined by the following formula: the number of subjects in whom cellular crescentic lesions were present in one specimen and absent in the other/the total number of subjects in whom cellular crescentic lesions were present, including those with lesions present in both specimens and those with lesions present in only one of the two specimens. The relationship between the total number of observed glomeruli in two specimens and the incidence of the presence of cellular crescentic lesions is shown in figure 1. The incidence of the presence of cellular crescentic lesions increased with the total number of glomeruli. When the number of glomeruli is > 30, the incidence of the presence of cellular crescentic lesions reached approximately 60%. The relationship between the number of glomeruli in the smaller specimens and the incidence of cellular crescentic lesions in one of the two specimens is shown in figure 2. In total, of 206 subjects, 105 contained cellular crescentic lesions in both or either specimen. The presence of
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