| The microscopic features shown in this photomicrograph is of a fungus commonly associated with: | View Page |
| Based on the structures observed in this photomicrograph, the most probable species of the fungus recovered from an induced sputum specimen is: | View Page |
| The fungus illustrated in this photomicrograph was recovered from an induced sputum specimen from a 74 year old man with chronic obstructive pulmonary disease. This isolate is most likely: | View Page |
| The dermatophytic fungus shown is in this photomicrograph, recovered from a ringworm lesion of the skin of the back of the hand of an 8 year old boy, was most likely contracted from: | View Page |
| An Aspergillus species was recovered from a sputum specimen of a patient with X-ray evidence of fungal pneumonia. Microscopic examination did not permit a species identification. A small amount of vegetative mycelium was removed and a direct mount prepared. The features indicated by the red arrows in this image are associated with which Aspergillus species? | View Page |
| The hyaline mold illustrated in this photomicrograph can be identified as: | View Page |
| A dull white fungus, turning mouse gray on maturity, was recovered from material aspirated from a bone cyst in the upper femur. Based on the microscopic appearance as seen in a lactophenol blue mount of a portion of the colony, the most likely identification is: | View Page |
| Illustrated in this photomicrograph are fruiting heads of Trichoderma species. Note the single, long, tapered phialides (red arrows), extending laterally from either side of the hyphae, one of the key identifying features of this fungus. Another hyaline mold that produces long tapered phialides is: | View Page |
| The fungus illustrated in this photomicrograph of a lactophenol blue-stained preparation was recovered from skin scrapings of a patient with tinea pedis. The most likely identification is: | View Page |
| Match each of the names of the fungal species listed with the corresponding identifying structures illustrated in the photomicrographs: | View Page |
| Match the names of each of the fungal species listed in the drop-down box with the corresponding identifying structures illustrated in the photomicrographs: | View Page |
| A presumptive identification of the four genera of slower growing pathogenic dematiaceous molds can be made by observing specific types of conidiation. Match the names of the species of dematiaceous pathogenic fungi with the corresponding microscopic features illustrated in the photomicrographs: | View Page |
| The fungal species most likely associated with the granulomatous infection seen in this photomicrograph, illustrating segmented, dark brown-staining grains with a giant cell is: | View Page |
| The infrequently encountered mold that is represented by the photomicrograph begins as a gray-white colony that blackens with maturity as the hyphae become darkened and single, globose, black conidia are produced. This fungus can be identified as: | View Page |
| The multi-celled conidia of this dematiaceous mold are divided into cells by what are called distosepta (pseudosepta), indicating that the individual cells are surrounded by a sac-like wall that is distinct from the outer cell wall of the conidium. The identification of this mold is: | View Page |
| The type of sporulation of the dematiaceous mold that is illustrated in this photomicrograph is called: | View Page |
| The chain of conidia illustrated in this photomicrograph, with the deep-staining truncated bases, are called annelloconidia, and are most characteristic of: | View Page |
| In this photomicrograph are observed several background dematiaceous hyphae within which is seen a long, flask-shaped, tapered phialide (arrow) that has a flat saucer-like terminus. This feature is most characteristic of: | View Page |
| The disease with which the dematiaceous fungus illustrated in this photomicrograph is most likely associated is: | View Page |
| The dematiaceous conidium illustrated in this photomicrograph was obtained from a tiny portion of dark colony that grew to maturity in six days. Spores incubated in a saline mount for four hours developed germ tubes from both terminal cells. The features observed confirm the identification of: | View Page |
| Match each of the names of the dimorphic fungal species with its corresponding mold form as seen in the photomicrographs. | View Page |
| The colonies shown in the upper image were obtained on blood agar from a sputum specimen after 10 days incubation at 30°C. The lower image is a photomicrograph of a lactophenol blue mount made from a portion of the colony. The diagnosis is: | View Page |
| The growth of the colonies shown in the upper image was obtained on blood agar from a sputum specimen after 8 days of incubation at 30°C. The lower image is a photomicrograph of a lactophenol blue mount made from a portion of the colony. The diagnosis is: | View Page |
| The colonies shown in the upper image, obtained from a biopsy of an ulcerating skin lesion of the arm, are growing on agar slants of Sabouraud's dextrose agar. The lower image is a photomicrograph of a lactophenol blue mount made from a portion of the colony growing in the left slant. The diagnosis is: | View Page |
| This image illustrates a lactophenol blue mount of a mold recovered after 7 days incubation of brain heart infusion broth. The large macroconidia suggests the mold form of Histoplasma capsulatum. However, there is the possibility that this mold represents its saprophytic counterpart, which is: | View Page |
| Match the names of each of the yeast species with its most likely colony morphology as seen in the images on the right. | View Page |
| The growth of the yeast-like colonies shown in the upper image was obtained on blood agar from a skin culture only in the area overlaid by virgin olive oil. The lower image is a photomicrograph of a lactophenol blue mount made from a portion of the colony. The disease associated with this fungus is: | View Page |
| The forms seen in this photomicrograph, produced from a light inoculum of an unknown yeast colony incubated in rabbit plasma at 35°C for 2 hours, leads to the presumptive identification of: | View Page |
| Shown in this photomicrograph is a Gomori methenamine silver stain of a lung biopsy obtained from a patient with X-ray evidence of multi-focal pneumonitis. The yeast most likely to be recovered in culture of this tissue is: | View Page |
| The colony shown in the upper image was recovered from peritoneal fluid of a patient receiving continuous peritoneal dialysis. The lower image is a photomicrograph prepared from a small portion of the colony illustrating the microscopic morphology. Each of the following species of yeast can be eliminated except: | View Page |
| A hematology technologist observed the intracellular forms seen in the field of view of a Wright-Giemsa-stained peripheral blood smear shown in this photomicrograph. In consultation, the microbiology technologist advised that the form seen most likely represents: | View Page |
| This photomicrograph is an acid-fast stained smear prepared from a yeast colony growing on ascospore agar. A helmet-shaped, red-staining, acid fast yeast cell is seen in the center of view at the tip of the arrow, against the background, blue-staining blastoconidia. The presumptive identification of Hansenula anomala was made. Predisposing conditions that may indicate that this isolate is more than a contaminant include: | View Page |
| Illustrated in this photomicrograph of a lactophenol blue preparation of a urine sediment is a cluster of yeast cells that were presumptively identified as Cryptococcus species. Further characteristics that may assist in confirming this identification are: | View Page |
| This photomicrograph is a representative field of a Wright-Giemsa-stained bone marrow aspirate in which a pair of budding yeast cells is seen centrally (arrows). Based on the appearance of these yeast cells, what other test would you expect to be positive? | View Page |
| The red cell inclusions in this split frame photomicrograph of peripheral smears are called: | View Page |
| G6PD deficiency A ten-year-old boy came to a physician's attention because of recent jaundice and icteric sclerae. The immediate laboratory work revealed: Hct 24%(normal 36%-47%), MCV 79.5 fl (normal 78-95fl),RDW 13%(normal 11.5-15.0%). His blood smear findings are reflected in these photomicrographs. Note particularly the spherocytes in the upper picture. Some resemble a half-blister with the other half of the cell containing solidly-staining hemoglobin. These are called eccentrocytes. When present, they should trigger a search for red cell hereditary G-6PD deficiency and the oxidant that triggered hemolysis. These morphological findings are only clues; specific testing for G-6PD deficiency should be performed. The blue arrows in the upper photomicrograph are directed toward solid-staining spherocytes in which the cell membrane is beaded by inclusions wrapped within the cell membrane, suggesting the remains of denatured hemoglobin. Included on the smear is a target cell, several acanthocytes, a smudge cell, and a few schistocytes. The lower photomicrograph is supravital staining of affected red blood cells, verifying the presence of Heinz bodies. This disorder was first recognized during the Korean war in 10% of black American soldiers given the antimalarial drug primiquine. | View Page |
| Intracellular RBC Inclusions-G6PD (continued) G6PD deficiency occurs in the same geographic distribution as malaria. It has been theorized that enzyme deficient cells are more resistant to malarial parasites than normal cells.When hemolysis is triggered, the appearance of the red blood cells is modulated by activity of the spleen.Spherocytes, schistocytes, and nucleated red blood cells may appear in the peripheral blood.Denatured hemoglobin removed by an active spleen may leave bite cells, identified by the arrows in this photomicrograph, suggesting the presence of G6PD deficiency. | View Page |
| Dimorphic RBC population Illustrated in the photomicrograph of a peripheral smear are two populations of erythrocytes. Approximately 50% of the erythrocytes are normal size and contain a full complement of hemoglobin. The patient had received blood transfusions. The transfused red blood cells are the normocytic, normochromic red cells. Admixed are microcytic erythrocytes and larger erythrocytes, some faintly mottled or smudged, suggestive of reticulocytes. This picture represents a hemolytic process with a reticulocyte response. A similar dimorphic red cell population appears following erythropoietin therapy. It is important to recognize when a population of cells in the peripheral smear is not in context with anticipated laboratory findings and the clinical situation. | View Page |
| After a review of the peripheral smear represented by this photomicrograph, which report is the most appropriate for documentation of the findings? | View Page |
| Howell -Jolly bodies/ other erythrocyte environmental alterations Several erythrocyte abnormalities are present in both the upper and lower photomicrographs. Many of these atypical cells are probably present as a result of the patient's splenectomy. Considerable anisocytosis and poikilocytosis with many tear-drop cells, bite cells, fragmented forms, and a few target cells are apparent. Some of the erythrocytes in the upper frame contain Howell-Jolly bodies (DNA fragments) that may be single or multiple, especially in myeloproliferative disorders. These inclusions stain negatively for iron and are eccentrically placed in the red cell cytoplasm. . | View Page |