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Case Collection2

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Title: Case Collection2


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Case Collection-2
  • Shashidhar.

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Thyroid Nodule
  • Fine-needle aspiration biopsy of a thyroid nodule
    in a 52 years-old man. The nodule is located in
    the lower pole of right thyroid lobe, it measures
    about 2.5 cm in its greatest diameter and is
    easily palpable the patient is euthyroid and
    apparently in good health.

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Discussion
  • Medullary carcinoma of thyroid (Shashi)
  • C cells calcitonin secretion.
  • Background shows amyloid.
  • Highly cellular aspirate, uniform nuclei.
  • Azurophilic granules in cytoplasm.
  • Later age (5-7th decade).

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Discussion by Author
  • This report illustrates a case of intrathyroid
    parathyroid carcinoma that masqueraded as a
    thyroid primary tumor both cytologically and
    clinically. The patient was first seen by an
    orthopedic doctor for evaluation of a back pain
    of increasing intensity. X-rays studies of the
    vertebral column and a laboratory blood test
    work-up followed. On physical examination a
    thyroid nodule was also palpated and the patient
    was seen by an endocrinologist. Ultrasound
    evaluation documented a solid, hypo-echoic nodule
    in the lower third of the left lobe of thyroid
    gland which was readily examined by FNA biopsy.

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  • On microscopic evaluation of the aspirate our
    first impression was that of a medullary thyroid
    carcinoma (MTC) but the following cytologic
    features seemed not to fit with the diagnosis
    uniform cell size and lack of significant
    cellular pleomorphism complexity of cellular
    arrangement with frequent three-dimensional tight
    clusters and tendency to cell aggregation
    abundant monomorphic naked nuclei concomitant
    presence of both oncocytoid and clear cells lack
    of spindled or triangular cells. Moreover, the
    tumor was located in the lower thyroid pole,
    which is unusual for MTC.

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  • In fact, cytologic features suggested a
    parathyroid lesion as an alternative diagnosis.
    Laboratory data which were made available soon
    after FNA biopsy sampling showed a calcemia of
    16.1 mg/dL, (n.v. 8.4-10.5), a phosphoremia of
    2.27 mg/dL (n.v. 2.5-4.5) and signs of slight
    renal insufficiency. These findings were
    consistent with a condition of hyperparathyroidism
    and strongly supported the above contention. Our
    FNA cytologic diagnosis was parathyroid tumor,
    uncertain if benign or malignant. Preoperative
    values of serum PTH were 2002 pg/ml (normal value
    8.0-76.0). The patient underwent right
    hemithyroidectomy with isthmus resection.

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  • Histology of surgical specimen demonstrated a
    well circumscribed and encapsulated intrathyroid
    nodule Foto_6 microscopically, the architecture
    of tumor growth was either solid structureless,
    or multinodular, or trabecular with thick fibrous
    bands incompletely dividing the tumor. The tumor
    consisted of a population of medium sized
    polygonal oxyphilic and transitional oxyphylic
    parathyroid cells Foto_7 with occasional mitotic
    figures. Immunostaining for PTH was positive
    Foto_8. There were occasional necrotic areas.
    Foci of capsular disruption and pericapsular
    invasion into thyroid parenchyma in addition to
    intravascular tumor growth Foto_9 and minimal
    foci of extrathyroid invasion were also seen.
    These latter findings demonstrated the malignant
    nature of the tumor.

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  • It is well known in the Literature that the
    distinction of parathyroid from thyroid cells in
    FNA samples can be challenging, and incorrect
    identification of parathyroid as thyroid lesions
    has been reported in a significant proportion of
    cases in the largest published series 1 2 3 4 5
    6. Potential trap is due to the finding in
    parathyroid lesions of aggregation patterns and
    cellular features, including intranuclear holes
    (cytoplasmic inclusions) 7, which overlap with
    those seen in thyroid follicular lesions 2 5 6 or
    Hurthle cell neoplasms 5 6, or papillary
    carcinoma 6 7. If the tumor exhibits a clear cell
    cytology it can be confused with a primary clear
    cell carcinoma of the thyroid. Naked nuclei can
    be misinterpreted as lymphocytes and suggest the
    diagnosis of lymphocytic thyroiditis 8. Finally,
    as in the present case, plasmacytoid or
    oncocytoid cellular morphology and intranuclear
    holes can simulate the FNA cytological picture of
    medullary thyroid carcinoma 6 9.

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Well circumscribed and encapsulated intrathyroid
nodule
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medium sized polygonal oxyphilic and transitional
oxyphylic parathyroid cells.
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Immunohistochemical expression for parathyroid
hormone.
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Intravascular spread.
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Case General Path,
  • 18 years old patient with polyadenopathies.
    Clinical suspicion of tuberculosis because of
    positive familial epidemiology.

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Lateral cervical lymph node in 75 years old male.
  • Antonio Félix Conde Martín
  • Servicio de Anatomía PatológicaHospital Can
    MissesC/ Corona s/n Ibiza07800 Baleares
  • Spain

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Clinical details
  • Male 75 years old with multiple bilateral
    cervical lymphadenopathies. A fine needle
    aspiration cytology is performed.

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Discussion
  • MALIGNANT NON HODGKIN HIGH GRADE B CELL LYMPHOMA
    (CENTROBLASTIC).
  • IHQ la población tumoral es de estirpe B-CD20,
    CD79a, prolifera con MIB1 en un 80, siendo p53
    positivo en un 10 de las células. CD10-, BCL-6,
    BCL-2 irregular. Quedan escasas células T
    preservadas y son abundantes los histiocitos
    CD68.

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Discussion
  • The smears are composed of a monomorphous
    population of cells with large nuclei with
    several nucleoli near the nuclear membrane and
    scant cytoplasm (centroblasts). According with
    these features the diagnosis of high grade non
    Hodgkin lymphoma was suggested. A lymph node
    biopsy is performed.
  • Histological sections show lymph node
    architectural effacement by medium to large size
    lymphoid cells with clear nuclei with prominent
    nucleoli and scant cytoplasm. The intestitium
    shares different degrees of fibrosis.

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IHC-Immuno histo-chem
  • the tumoral population is B-cell lineage CD20,
    CD79a. Proliferation index 80 (MIB1). p53
    positive in 10 of cells. CD10-, BCL-6. BCL-2
    irregular positivity. Seldom T cells preserved.
    Abundant CD68 histiocytes.

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Thank You!
  • First of all thank you very much to all those who
    have participated with your commentaries. It is
    very stimulating for us to know that every week
    we count on so many and so great pathologists at
    this forum.

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Man with acute abdomen.
  • E-medicine
  • Image case

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History
  • This 42-year-old man presents to the emergency
    department after approximately 30 hours of
    abdominal pain. The patient's pain was initially
    mild, constant, and periumbilical, lasting nearly
    10 hours before resolving. After he ate
    breakfast, the pain returned to the right lower
    quadrant and gradually progressed over the next
    20 hours.

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History
  • The patient denies any fever, nausea, vomiting,
    diarrhea, constipation, bloody stools, weight
    loss, testicular pain, or anorexia. Physical
    examination reveals an afebrile, well-appearing
    man with localized voluntary guarding and rebound
    tenderness in the right lower quadrant. In
    addition, he has positive heel tap, Rovsing, and
    psoas signs. Contrast-enhanced CT of the abdomen
    and pelvis is performed (see Image A). What is
    the diagnosis?

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Discussion
  • Although the patient's presentation is classic
    for appendicitis, he lacks some findings on
    review of systems. He was in no distress and
    afebrile, without any anorexia or vomiting.
    Initial CT of the abdomen showed a thickened
    terminal ileum a normal-appearing appendix and
    perimesenteric fat stranding, which was read as
    nonspecific inflammation of the bowel most
    consistent with regional enteritis. However,
    because his pain worsened over the next several
    hours, he was taken to the operating room for
    diagnostic laparoscopy. As shown on the
    intraoperative image (see Image B), a toothpick
    was found perforating the cecum. The toothpick
    was removed, and the patient had an uncomplicated
    recovery.

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  • Toothpick ingestions are rare, but the literature
    includes several case reports. Approximately 70
    of patients with reported toothpick ingestions
    present with abdominal pain. However, only about
    12 remember ingesting the toothpick. The onset
    of symptoms varies, with a reported range of less
    than 1 day to 15 years after ingestion.
    Perforation frequently occurs at the duodenum
    and sigmoid, but this case shows it may occur
    anywhere. Imaging studies are useful in only 14
    of cases laparotomy is the most common method
    for definitive diagnosis. The overall reported
    mortality rate is as high as 18 (Li, 2002).
    Patients ingesting sharp objects and objects
    larger than 2 X 5 cm should be watched closely
    and treated aggressively.

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  • This case reminds physicians that a CT may be
    bypassed in a patient with a surgical abdomen.
    Although the patient lacked some classic symptoms
    of appendicitis, the history and examination
    findings were consistent with a surgical abdomen.
    CT may have delayed the appropriate treatment,
    which was diagnostic laparoscopy.

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Gen-Path Uninethttp//pat.uninet.edu/zope/pat/c
asos/C144/index.html
  • 18y Female Cervical lymphadenopathy

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Clinical Details
  • Female, 18 years old with multiple right
    lateral-cervical lymph node painless enlargement
    lasting for more than one month, without any
    other clinical sympthoms. A lateral-cervical
    lymph node biopsy is performed.
  • lymph node 1,5 cm in largest diameter. The cut
    surface shares regular yellow areas intermingled
    with normal appearing areas among them.

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44-year-old woman, previosly healthy, presented
with chest pain (right side), fever, cough and
mucoid expectoration. Physical examination was
unremarkable. Chest x-ray showed subpleural
nodular (6x4x4 cm) shadow in right lower lobe. A
lobectomy was performed.
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Subpleural Nodule Biopsy
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Sub pleural Cryptococcoma
  • Cryptococcus neoformans is an encapsulated yeast,
    round or oval (3.5 to 8.0 microns).
  • Narrow based budding is observed between the
    parent and daughter cells (blastoconidia or
    buds).
  • Cryptococcus neoformans is the most common human
    pathogen.
  • Four serotypes (A,B,C,D) of Cryptococcus
    neoformans A and D common.
  • Cryptococcus neoformans classically is associated
    with desiccated pigeon feces, can be found in the
    feces of other birds.

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Discussion
  • Inhalation of fungus leads to infection of the
    lungs.
  • A transient colonization of airways or more
    extensive pulmonary involvement.
  • May be self-limited or a progressive pulmonary
    disease.
  • May disseminate to other sites common
    meningitis. 85 meningitis cases may not have
    pulmonary symptoms.
  • The final result of pulmonary infection may be a
    cryptococcoma or a residual pulmonary nodule.

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35 Year male with Jaundice Weight
loss.http//path.upmc.edu/cases/case297.html
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History
  • 35-year-old Asian man from Thailand.
  • Jaundice, fatigue, Wt loss 15 pounds/2mon
  • LFT - AST 121 IU/L, ALT 112 IU/L, ALP 539 IU/L,
    GGTP 570 IU/L, Bil Total 13.5 mg/dl, direct
    bilirubin 10.1 mg/dl.
  • CT scan demonstrated 1) multiple hepatic and
    pulmonary lesions 2) dilatation of bilateral
    hepatic ducts and common bile duct with thickened
    walls and infiltration of periportal soft
    tissues 3) large volume of ascites 4)
    heterogeneous and nodular omentum

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Imaging Investigations
  • Multiple hepatic and pulmonary lesions
  • dilatation of bilateral hepatic ducts and common
    bile duct with thickened walls and infiltration
    of periportal soft tissues
  • large volume of ascites
  • heterogeneous and nodular omentum

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Imaging Investigations
  • ERCP revealed multiple strictures in the intra-
    and extra-hepatic biliary system
  • Tumor marker CA19-9 320,000 U (ref lt38.0 U)
  • CEA 52 ng/ml (ref lt5 ng/ml).
  • Alpha-fetoprotein - normal

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Bile and Ascitic fluid cytology
  • clusters of small, yellow-brown, urn-shaped
    parasitic ova with a convex operculum resting on
    "shoulders" and a small knob at the opposite end.

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Bile fluid cytology
  • loose clusters of atypical ductal epithelial
    cells
  • Nucleomegaly, hyperchromasia, coarse chromatin
    and irregular nuclear membrane

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Final Diagnosis
  • Cholangiocarcinoma, secondary to infection of
    liver flukes (Clonorchis sinensis or Opisthorchis
    viverrini).
  • Humans are infected by eating raw or undercooked
    fish containing the encysted larvae
    (metacercariae).
  • After excystation in the duodenum, the immature
    flukes enter the biliary ducts and differentiate
    into hermaphroditic adults which produce eggs
    released into feces ? snails ? Fish.
  • The adult fluke has a life span of more than 20
    years, which explains persistent infection.
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