Overview of Bone Marrow Aspiration from 120 Cats in Different Hematological Conditions

Bone marrow (BM) evaluation is highly important for the diagnosis of numerous hematological alterations in animals, especially cats, given their greater propensity for hematopoietic changes associated with retrovirus infections. This study aims to describe the main aspects of the BM of cats with different hematological conditions, comparing with reference intervals established from animals without hematological alterations and also with a previously established reference interval. To do so, we evaluated full blood and BM samples from 120 cats with no abnormalities on physical examination, negative for FeLV and FIV. Hemograms were performed from automated total cell and platelet and leukocyte differential counts in blood smears. BM samples were placed in Petri dishes; medullary spicules were selected to make up to eight cytological slides stained by the May–Grunwald–Giemsa technique, which were subjected to quantitative and cellular morphology evaluations. The cats were predominantly young, 64.2% female and 35.8% male. The average number of medullary spicules in samples was 13.7%, and density was 44%. In the BM quantitative analysis, prorubricytes and rubriblasts had higher quantities than the recommended one for all cats with or without hematological alterations. In all groups, lymphocytes were decreased, and cats with lymphocytosis were closest to the reference range, showing flame cells and Mott cells. The reference interval for the bone marrow cell count obtained from the samples in this work differs from previously established data, leading to different interpretations of the patient's BM condition, according to the cell population observed and the reference interval used. This divergence strongly emphasizes the need to correlate clinical, epidemiological, hematological, and bone marrow data of each patient for a better understanding of the patient's condition. The popularization of BM assessment is essential so that more reliable reference intervals can be established according to the population served by each pathologist and clinical laboratory.


Introduction
Bone marrow evaluation is a valuable resource to identify diseases associated with the production, maturation, and release of erythrocytes, leukocytes, and megakaryocytes (MKs).It allows us to identify changes in such cells directly at their site of origin [1,2].In veterinary medicine, despite being a diagnostic tool not often listed by the clinical community, BM aspiration is more commonly used than biopsy due to its faster analytical speed and ease of sampling [1,3].
Bone marrow examination should be performed in conjunction with hematological evaluation and consists of two main and complementary analyses, morphological and quantitative [2][3][4].Te former seeks to characterize cells in terms of morphology, identifying cytoplasmic and nuclear alterations, while the latter seeks a broad view of medullary composition, indicating numerical variation of precursor cells and their subsequent lineages [2].
In cats, BM evaluation is recommended in cases of persistent regenerative anemia, neutropenia, and thrombocytopenia, as FeLV Combo Test, IDEXX Laboratories, Inc., Westbrook, Maine, USA) and additionally for FeLV by polymerase chain reaction (PCR).FeLV proviral DNA was amplifed based on the U3 LTR region and gag gene of FeLV subgroup A. Of the 188 cats evaluated, 49 were positive for FeLV and two mutually positive for FeLV and FIV.
Blood for a complete blood count (CBC) was collected by jugular venipuncture, and samples were stored in tubes with EDTA for a maximum of 5 hours in refrigeration (ranging from 4 to 8 °C) until the moment of analysis.Hematocrit was determined by the microhematocrit method.A total count of erythrocytes and leukocytes was performed using an automated cell counter (SDH-3 Vet, Labtest, Lagoa Santa, Minas Gerais, Brazil).Te diferential leukocyte count and estimated platelets were counted from stained blood smears with rapid hematological stains (Newprov, Pinhais, Paraná, Brazil).Evaluation and interpretation of changes in the CBC were performed using reference intervals (RIs) established by Weiss and Wardrop [8] since these are the RI values routinely used in the sampled region, and no specifc criteria were used to establish an interval for hematology from the animals evaluated in this research.
For BM sampling, the cats were maintained under general dissociative anesthesia with ketamine and xylazine by intramuscular (IM) injection at 10 mg/kg and 1.5 mg/kg, respectively.Tramadol (2 mg/kg/IM) was used as a preanesthetic medication, and preventive antibiotic therapy was made with benzathine penicillin (24 mg/kg/IM).After the sampling, the patients rested until complete anesthetic recovery, followed by surgical discharge.Te patients were followed up by telephone contact with the tutors and returned after seven days for removal of the sutures of the neutering procedure and general clinical evaluation.None of these patients showed any relevant alterations from the immediate postoperative period until the removal of the stitches.
Bone marrow samples were collected from the left deltoid tuberosity using standard Jamshidi trifaceted or Illinois beveled cannulas, with a Luer-Lock closure system and size of 16G (0BIL1617/080 ™ and BIL1617 ™ , Biomedical Srl, Firenze, Italy).Aspiration was performed using 5-10 mL syringes coupled to the cannula, to obtain 0.3-0.8mL of BM.At least fve and at most eight marrow smears were prepared per patient using the squash technique, depending on the number of spicules obtained.All smears were stained using the May-Grunwald-Giemsa (MGG) technique diluted in Sorensen bufer.Te smears were frst evaluated according to the number of spicules per smear (×100), density and cellularity of spicules (number of precursors/adipocytes), degree of maturation of precursors, and quantity of lymphocytes and plasma cells in every fve felds of higher magnifcation (×400).
A cytomorphological evaluation was performed according to Harvey [1].Megakaryocytes were carefully evaluated at 100x magnifcation in 10 felds of the perispicular and spicular region.Quantitative diferential evaluation of BM was performed on the two best smears of each animal, which were free of artifacts and without excessive cellular overlap, by counting 500 nucleated cells (NCCs) at 1000x magnifcation in immersion, with the aid of a light optical microscope.Te counts were cataloged and calculated using the BM conter©2008 smartphone application (Kazuyoshi Sasaoka, AppStore).
Te diferential cell count was performed in hot spots on the periphery of spicules, having reference values as previously described by Jain [5] and the NCC of the cats evaluated in this research free of clinical and hematological alterations.Among all the collected samples, 17 had NCC lower than 500 or showed marked platelet aggregation and, therefore, were excluded from the analysis.Cells were 2 Veterinary Medicine International carefully evaluated for size, maturation degree, cytoplasmic color, nuclear shape, nuclear segmentation, chromatin arrangement, and cytoplasmic and cytoplasmic membrane characteristics, with any changes being described as prescribed by Harvey [1].Te bone marrows were considered regular if they showed cellularity ranging between 25% and 75% concerning the number of precursors/adipocytes, widely dependent on the age of the animal in question, in which the myeloid to erythroid ratio (MER) decreases proportionally with advancing age.Tese results were always analyzed in conjunction with the CBC of the respective patient.
Due to the limitations of this research, the promoting factors of the patient's hematological alterations were not investigated.Tus, the groups for comparison were composed solely according to the alteration observed, without focusing specifcally on the cause.For comparison with BM obtained data, the evaluated animal groups were selected and separated according to hematological condition in cats without hematological abnormalities, anemic, with neutrophilia, eosinophilia and basophilia, lymphocytosis, monocytosis, and lymphopenia, considering that the same animal could be part of more than one group.
Te samples of BM, blood, and epidemiological data used in this manuscript came from a sample from another research project carried out by the same authors, which was approved by the Committee on Ethics in the Use of Animals (CEUA) of the University of Santa Catarina State (UDESC), with registration 2306130319 (ID 000831).In addition, an informed consent form was signed by the owners authorizing the use of the samples and data provided.
As for the overall analysis of 120 BM aspirates, the number of spicules per sample ranged from 1 to 50 per slide, with an average of 13.7 (±8.7), and density between 25% and 80%, with an average of 44% (±15.3).Te average number of spicules in young animals was 8.1 (±5.1), with an average density of 42.1% (±14.1); in adult animals, the number of spicules reached an average of 16.3 (±7.2) and an average density of 56.7% (±50).Te count of MK showed an average of 16.9 (±8.8) cells per ten low-power felds (10x objective) and that of lymphocytes had an average of 5.31 (±1.8).In rare cases, MKs with neutrophil emperipolesis were observed.
None of the animals submitted to this study presented any illness at the time of sampling or afterward.During the telephone follow-up carried out with the tutors, none of the patients had changes in their health status or behavior after the procedure, until the removal of the suture stitches.

Cats with Hematological
Changes.Tis group comprises the animals that presented some hematological alterations, even in the absence of clinical signs or a history of previous illnesses.None of these patients developed a clinical disease until the end of the postsurgical period, nor did the tutors seek clinical care or report any abnormal health conditions in the patients until the completion of this project.

Anemia.
Te two cats that had changes compatible with anemia were males, young, aged 24 months old.Te cause of anemia was not investigated, as these patients had no history or evident clinical alterations at the time of obtaining the samples, one of them with normochromic normocytic anemia (Cat 1) and the other with normochromic microcytic anemia (Cat 2), as shown in Table 3, both without relevant leukocyte alterations, in addition to mild eosinophilia.Neither of the two samples underwent reticulocyte counts at the time of CBC.
In both patients, the erythroid lineage was superior to the myeloid, with a special prevalence of prorubricytes (11.6% and 9.8%), about ten times higher than that recommended by Jain [5] and slightly increased about to the values obtained in the hematologically healthy animals of this Veterinary Medicine International   Of the 22 animals, 21 had numbers of intramedullary neutrophils above the maximum indicated for the reference interval, which is compatible with a picture of granulocytic hyperplasia of the neutrophilic order.However, using the values obtained in the 57 cats free of hematological alterations as a reference, the number of intramedullary neutrophils is found in values considered within a normality threshold, despite the average value of rods being slightly increased.A general marrow analysis of cats with neutrophilia can be seen in Table 5.

Eosinophilia and Basophilia.
Increased numbers of circulating eosinophils were identifed in 19.2% (23/120) of cats.Of these, 78.3% (18/23) were females and 21.7% (5/ 23) were males.Te average age of these animals was 20.6 (±13.9)months, among which young cats accounted for 73.9% (17/23) of cases.Tese cats had no changes in the erythrogram; however, 12 (52%) had leukocytosis (19.960 to 35.550/µl).Te average amount of eosinophils observed in these patients was 2.827/µl (±1.692).Quantitative analysis of the BM in these cats was very similar to that in neutrophilia patients, except for prorubricytes (× 6.8% ± 2.9) and the sum of the average number of eosinophilic lineage cells ( × 3.8%), both increased when compared to the previously reported RI.In the data obtained from the hematologically healthy patients, the eosinophil precursors were separated according to each specifc cell type, and when comparing patients with eosinophilia with these data, no relevant quantitative changes were observed.
Among cats with eosinophilia, there were still two previously mentioned cases of anemic animals with erythroid hyperplasia (8.7%, 2/23) and 21 (91.3%)cases of granulocytic hyperplasia of the neutrophilic order.Among these 21, eight (38.1%) also had several intramedullary eosinophils (summing up all maturation phases) higher than the recommended reference interval determined by Jain [5], but not concerning the reference established in this research, as can be seen in Table 6.
Quantitative analysis of the BM in these patients was similar to that previously mentioned, with a clear increase in the number of erythroid lineage cells, if the recommended reference was used, however, without changes when using the one established by the animals without hematological alterations in this research.Despite basophilia, there was no increase in the average of basophil precursors (× 0.3% ± 0.3) compared to animals with no one or other hematological conditions.Te analysis also showed that, among these cases, 14 (93.3%) had neutrophilic granulocytic hyperplasia as recommended by Jain [5], in addition to those with erythroid hyperplasia.
Compared with the previously established reference intervals, the evaluation of the bone marrow of these animals showed increasing numbers of myeloblasts (× 1.5% ± 0.7), promyelocytes (× 3.1% ± 1.6), and neutrophils (× 25.9% ± 2.4).Conversely, for erythroid lineage cells, only prorubricytes had higher numbers, averaging 5.7% (±2).Lymphocytes were also not abundant in BM smears, but intramedullary lymphocytes had a number closer to that recommended by Jain [5], with an average of 10.2% (±4).Te reference instituted from the use of data from cats in this research did not demonstrate relevant quantitative alterations in any of the aforementioned cells.Te general appearance of the bone marrow of these animals is shown in Table 7.
Moreover, four of these cats (50%, 4/8) had discreetly increased plasma cells in the marrow, ranging from 1.6 to 2.4% (× 2% ± 0.4), according to Jain [5], but not with the values established in the research.Flame cells could also be identifed in these cases (Figure 2(a)) and Mott cells in two cases (25%) (Figure 2(b)).
Leukocytosis was detected in 10 (83.3%) of these animals, in which, in addition to monocytosis, neutrophilia predominated (9/12; 75%), followed by eosinophilia (8/12; Veterinary Medicine International 66.8%), basophilia (6/12; 50%), and lymphocytosis (2/12; 16.8%).Cytological evaluation of the BM revealed monocyte values higher than the maximum limit of the reference used (0.0-0.2), ranging from 0.4 to 2.2%, with an average of 1.6% (±1.1%).Only one patient had a monocyte percentage of 2.2%, higher than the reference interval established by the authors of this manuscript.In one case, a large number of neutrophils were recorded.Te diferential count of the evaluated cells is better described in Table 8.   6 Veterinary Medicine International

Veterinary Medicine International
Te average total lymphocyte count in BM aspirates was 8.2% (±3.1), ranging from 1.2% to 13.6%.Among medullary smears from these cats, only two (11.76%) had lymphocyte values within the expected by Jain [5], all the others showed lower values, and furthermore, some of these animals also had concomitant monocytosis.Tese data contrast with the interval values obtained by the authors, which range from 6% to 12% and cover 13 of the lymphopenic animals.No morphological anomalies were observed in lymphoid, myeloid, or erythroid precursors, in any of the 17 marrow samples.Te general appearance of the BM of these cats is shown in Table 9.

Discussion
As for the general evaluation of aspirates, our fndings showed that the number of medullary spicules was higher in adult animals, contradicting what was expected when considering the physiological characteristics of patients [1].Younger cats are known to have greater medullary activity  8 Veterinary Medicine International  Veterinary Medicine International and availability of spicules for evaluation [1,18].However, in this study, kittens showed a smaller number of spicules in the sample than other age groups.It is also important to point out that factors such as the technique and sample obtained may also infuence this result.Artifacts in the manufacture of slides can compromise the distribution of cells, culminating in intense overlapping, crushing, and countless others, signifcantly interfering in the analysis [19].Samples of males had a higher number of viable spicules than those of females.A study in humans evaluating BM aspirated nucleated cells identifed a progressive reduction in their number with advancing age; however, no signifcant diferences were reported between the sexes [20].So far, no studies have discussed variations in the number of spicules between sexes and age groups in cats.For us, the relationship between these factors and counts of spicules in samples is unlikely, thus occasional fnding.
In adult cats, MKs were numerically superior to those in other age groups.Tis fnding was also reported in a study on megakaryocytic activity in mice; the authors believed that it is related to an increase in thrombopoietin activity and its respective receptor [21].In rare cases, emperipolesis of neutrophils could be observed in mature megakaryocytes, as already described in humans [22].Te process is still poorly understood but is believed to be linked to the limited space restriction in the BM, or even the access to the circulation route [23][24][25].In addition, MK emperipolesis can be observed in myeloproliferative diseases, involving distinct leukemia [26,27].However, those alterations were not diagnosed in the animals in our study.
Te 57 cats without hematological changes had total marrow cell counts diferent from those described by Jain [5].Tey also difered from those found by Turinelli and Gavazza [11], in a retrospective study where the most evident discrepancy was for total values of myeloid and erythroid precursors.
In our study, in turn, these were about 10% higher for myeloid lineage and 10% lower for the erythroid one.Although physically healthy, most of the animals evaluated in this study came from routine neutering made in ZCC-Lages.Tis surveillance center serves, for the most part, a socially vulnerable population; thus, control and prophylaxis measures against animal diseases are uncommon.Because of this, such constant and intense exposure to immunological challenges is speculated to promote continuous stimulus to granulopoiesis [1,2,9].As the sampling was carried out in a single moment, subsequent samples were not collected for comparison purposes, limiting the evaluation of the evolution of the hematological condition of these patients.
Environment-related hematopoietic changes have also been described in sheep exposed to high temperatures [28].Still, no study has assessed the infuence of environmental factors on cats.Terefore, granulopoiesis observed in our study seems to be an adaptive response to the environment where these animals lived, increasing numbers of intramedullary myeloid precursors.
Te MER in animals without hematological changes ranged from 0.9 to 2.24, with the minimum being lower than the recommended one (1.21)[5].Tis result may lead the evaluator to consider a condition compatible with erythroid hyperplasia or granulocytic hypoplasia.Tus, MER must be judiciously evaluated and in association with other medullary, hematological, and clinical alterations to determine the existence of a disease associated with the condition or if these results are inherent to the patients themselves [29,30].Other studies on normal cellularity in the BM of cats reported MER values even lower than those found in this work, ranging from 0.31 to 0.6 [11,12].It is also noteworthy that the reference interval reported by Jain [5] is based on a small number of animals from a specifc region.
Another important observation is related to the average number of eosinophilic precursors in these cats, which together exceeded the maximum stipulated by Jain [5] by about 25%.Studies have revealed that hyperplasia of this lineage can only be determined when precursor values exceed 6% of the neutrophil count [1,2,9,11].Tis fnding, therefore, was not considered relevant when evaluated in conjunction with the blood count.Furthermore, these precursors were typical and without signifcant morphological, nuclear, or cytoplasmic alterations that are indicative of dysgranulopoiesis [4,9].It is also not possible to rule out that such an alteration is simply physiological and transitory.
Both anemic patients exhibited reactive erythroid hyperplasia, indicating a marrow response.Tis feature requires at least four days to occur, a period required for erythropoietin action to be efcient.It is said that such conditions can be determined by low MER values, in association with a large number of nucleated erythrocytic cells in aspirates, among which rubricytes and metarubricytes predominate [9].It difers from what was observed by the authors, in which rubriblasts had larger amounts.Such a hyperplastic response, associated with anemia, may represent a subclinical chronic disease, which can range from iron defciency to progressive renal diseases [5,8,31].Nevertheless, a more assertive diagnosis was limited by the method used in this research.
Neutrophilic cats, in turn, showed MER within the reference range, but the average of intramedullary neutrophils was above the standard.Terefore, these cats could be characterized as carriers of neutrophilic granulocytic hyperplasia [5,9].Such an alteration may require more days to signifcantly alter MER [9], which could explain why values remained within the prescribed range and the hematological healthy animals in this research.However, the absence of clinical and hematological features of infammatory and infectious processes, in most of the evaluated cats, makes us question whether granulocyte values prescribed for hyperplasia diagnosis are overestimated.
Te number of intramedullary or circulating neutrophil precursors showed no changes.In this way, such hematological fndings can be associated with the conditions in which animals remained from transport to sample collection.Tey were far from their natural environment, sharing space with people and animals diferent from usual, and being subjected to climate changes, mechanical restraint, and manipulation [32][33][34].
Eosinophilia and basophilia were observed in multiple patients.However, they cannot be attributed solely to 10 Veterinary Medicine International physiological leukocytosis, as the parasite load and history of allergic diseases or hypereosinophilic syndromes were unknown by their owners.Studies have described those helminths, autoimmune syndromes, and allergic diseases are the main promoters of these hematological changes.Moreover, stimulation of granulocytic colonies of eosinophils and basophils (GC-Eo/B) by interleukin 5 (IL-5) action may or may not increase eosinophilic cellularity [5,[33][34][35][36][37].
Few studies numerically exposing normal cat marrow have pointed to a wide variation in intramedullary eosinophilic precursors but with an average of no more than 3.2% of NCC [5,11,12].Interestingly, cats without hematological alterations had a higher number of intramedullary eosinophilic precursors.Tis result led us to question whether the reference range of these cells for cats is not strongly dependent on the living conditions and habitat of the patients, as previously discussed.Tis is because it induces a physiological need for a greater supply of eosinophils.Tis hypothesis is based on data from another study, which showed a maximum of 7% for eosinophilic lineage cells in animals with BM under normal conditions [11].It contradicts the values previously defned to consider eosinophilic hyperplasia [7,9].
Te marrow response in cases of lymphocytosis was also not expressive in any of the cats evaluated in this study.Of the eight animals with such an alteration, four showed a simultaneous increase in neutrophils, in line with what is expected in the case of lymphocytosis due to excitation [32][33][34].Although lymphocytosis is often a nonspecifc fnding, it may also be associated with viral infections, hemoparasites, and mild infammation, or with certain chronicity [33,34] and even chronic lymphocytic leukemia (CLL) [38,39].
Under conditions described as normal, marrow lymphocytes can vary from fve to 21.6% of NCC [2,5,30], which is in line with the data found in this research.Tese values seem to be high when compared with older data, which estimated an average of 5% of lymphocytes in the BM [12], as well as in the reference instituted by the authors in the elaboration of this research; however, they are close to the average value found by other authors [13].According to the literature, mature lymphocytes are easily confused with erythroid precursors due to their size and shape [2,29,30].However, we emphasize the need to pay attention to cytoplasmic features and erythroid cell nuclei, which tend to be intensely basophilic and with more compacted chromatin, as described by other authors [4].
Mott and fame cells, which are deemed as reactive forms of plasma cells, were observed in cats with lymphocytosis in moderate amounts, with the fame cells being the most numerous.Flame cells consist of larger than usual plasma cells, with reddish inner cytoplasmic membranes due to the accumulation of carbohydrate-rich immunoglobulins, predominantly IgA [2,39].Both fame and Mott cells have been observed as primary components of leukemia in humans [40], as well as in monoclonal gammopathies [41] and myelomas in dogs and cats [42][43][44].Tese patients showed no clinical changes that could indicate the existence of the mentioned diseases.However, due to a limitation of this study, complementary tests with greater specifcity were not performed to confrm or exclude those diagnoses, such as the detection of Bence-Jones protein in urine, as well as imaging and serum biochemical evaluations [45,46].
Te same is discussed for the 17 cats showing isolated lymphopenia, without reduction in other circulating cells.Tere are numerous causes for this, among them viral diseases, rupture of lymphatic ducts, neoplastic processes that alter the structure of lymphatic organs, and use of immunosuppressive drugs [33,34,47,48].However, none of the cats showed clinical or historical alterations that could support these causes.Furthermore, it is relevant to mention that 13 of these patients had lymphocyte values similar to the reference interval established by the authors, which makes the idea that the number of previously established lymphocytes does not globally represent patients of the feline species feasible.An exception may be viral infections since; in this work, animals were only tested for FeLV and FIV.
Such patients had a lower number of intramedullary lymphocytes than the recommended reference [5].However, besides being within the values established as a reference by the authors, some researchers have characterized marrows as normal when the number of lymphocytes ranges from 1.5% to 28.5% [11], while others have considered a range from 5% to 20% [29].

Conclusions
Te reference interval for the BM cell count obtained from patients without hematological alterations evaluated in this study difers from previously established data, which may be associated with several intrinsic factors, from individual characteristics to the home environment and life habits.
Tis divergence leads to multiple diferent interpretations of the condition of the patient's BM, according to the cellularity present in the sample and the reference interval used.Tis strongly emphasizes the need to correlate the clinical, epidemiological, hematological, and BM data of each patient for a better diagnostic defnition.
Although this work does not intend to determine new reference intervals from the evaluation of animals without hematological alterations, it is believed that it can serve as a complement in the study of the BM of some specifc patients.In addition, it is observed that BM evaluation should be more popularized, familiarizing clinicians with sampling methods and benefts brought to patients with hematological disorders.From this, it is believed that more reliable references can be established according to the population assisted by each pathologist and clinical laboratory.

Figure 1 :
Figure 1: Bone marrow aspirate from a cat with erythroid hyperplasia.(a) Rubriblasts (black arrows) in moderate quantity, followed by a large number of rubricytes (black arrowheads) at diferent maturation stages, and a large granulocytic precursor in typical metaphase (red arrowhead) (400x, MGG).(b) Approximate image A in which increasing proportions of rubriblasts (black arrow), prorubricytes (black arrowhead), and multistage rubricytes can be seen regarding granulocytic precursors, such as myelocytes (red arrow) and rod neutrophils (arrowhead red) (1000x, MGG).

Figure 2 :
Figure 2: Bone marrow aspirates from cats with lymphocytosis.(a) Abundant plasma cells with the irregular cytoplasmic membrane and cytoplasm with intensely pinkish margins, characterizing fame cells (black arrow).(b) Large plasma cells flled with optically empty vesicles of similar size (Russell's corpuscles), characterizing a Mott cell (black arrow) (1000x, MGG).

Table 1 :
Complete blood count values of 57 cats with no hematological alterations submitted to bone marrow aspiration.

Table 2 :
Descriptive analysis of the quantitative evaluation of bone marrow aspirates from 57 cats without alterations in complete blood counts.

Table 3 :
Red cell count values of 2 cats with anemia submitted to bone marrow aspiration.

Table 4 )
. Both patients had MER below 1 (0.95 and 0.88, respectively), contrasting with the values indicated in the recommended and self-instituted references.Te erythroid lineage showed reactive hyperplasia in both cases (Figures1(a) and 1(b)).

Table 4 :
Quantitative results of cytology evaluation of bone marrow aspirates from two clinical health cats with anemia.
1 Standard deviation.* Reference previously published by Jain [5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.

Table 6 :
Quantitative results of the cytological evaluation of bone marrow aspirates from 23 clinically healthy cats with eosinophilia and basophilia.
[5]andard deviation.*Referencepreviously published by Jain[5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.

Table 5 :
Quantitative results of the cytological evaluation of bone marrow aspirates from 22 clinically healthy cats with neutrophilia.
[5]andard deviation.*Referencepreviously published by Jain[5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.

Table 7 :
Quantitative results of the cytological evaluation of bone marrow aspirates from 8 clinically healthy cats with lymphocytosis.
1 Standard deviation.* Reference previously published by Jain [5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.

Table 8 :
Quantitative results of the cytological evaluation of bone marrow aspirates from 12 clinically healthy cats with monocytosis.
[5]andard deviation.*Referencepreviously published by Jain[5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.

Table 9 :
Quantitative results of the cytological evaluation of bone marrow aspirates from 17 clinically healthy cats with lymphopenia.
[5]andard deviation.*Referencepreviously published by Jain[5].* * Reference interval established from the values found in the 57 cats without hematological alterations evaluated in this work.