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Pancreatic Cytopathology - David C. Chhieng, Edward B. Stelow

Pancreatic Cytopathology (eBook)

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2010 | 2007
XI, 197 Seiten
Springer US (Verlag)
978-0-387-68947-0 (ISBN)
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Designed to be concise and easy to use, this volume focuses on pancreas cytopathology. It is the ideal companion for practitioners on the move. It is published in the Essentials in Cytopathology book series and fulfills the need for an easy-to-use and authoritative synopsis of site specific topics in cytopathology. These guide books fit into the lab coat pocket, ideal for portability and quick reference. Each volume is heavily illustrated with a full color art program, while the text follows a user-friendly outline format.


Diagnosis by cytologic means is what the mathematicians would describe as elegant; the methods are often simple but richly nuanced, while the results can be profound though succinctly stated. Tiny samples atraumatically obtained are at the heart of both the elegance and the dif? culties of this subspecialty. Following initial successes of traditional exfoliative cytology, further applications were long constrained by the fact that few body surfaces present themselves for direct collection of exfo- ated cells. Thus, it was inevitable that advances in nonoperative evaluations for speci? c body sites would be accompanied by expansions in cytologic diagnosis. Hence the proliferation of sampling methods with techniques the same as their names, including brushing, washing, lavage, and aspiration. Examples come readily to mind. One of the most dramatic bursts in cytodiagnosis happened in the 1980s, when deep-lung sampling by bronchoalveolar lavage (BAL) arrived at about the same time as the AIDS pandemic. Frequent and often repeated diagnosis of CMV and pneumocystis quickly led to numerous such samples being submitted to many laboratories. These now common infectious agents and this new technique were highly suited to rapid evaluation of AIDS patients. The rapid rise of ? ne needle aspiration occurred at about the same time, at least on this side of the Atlantic. Although not really new, the explosion in its use had awaited both cli- cal acceptance and adequate training for a critical mass of pathologists. This history has been well recorded by others.

to Pancreatic Cytopathology.- Pancreatic Cytopathology: A Pragmatic Approach.- Pancreatic Ductal Adenocarcinoma and Its Variants.- Ancillary Testing for the Diagnosis of Pancreatic Ductal Adenocarcinoma.- Acinar Cell Carcinoma.- Pancreatoblastoma.- Solid-Pseudopapillary Neoplasm.- Pancreatic Endocrine Tumors.- Cystic Muscus-Producing Neoplasia: Intraductal Papillary Mucinous Neoplasms and Mucinous Cystic Neoplasms.- Other Cystic Lesions of the Pancreas.- Inflammatory Disease of the Pancreas.- Secondary Malignancies of the Pancreas.

"7 Solid-Pseudopapillary Neoplasm (p. 95-96)

Also known as solid-cystic tumor, papillary-cystic tumor, and solid and papillary tumor of the pancreas, this low-grade primary pancreatic epithelial neoplasm accounts for 1% of all exocrine pancreatic neoplasms. It occurs predominantly in adolescent girls and young women and is rare in men and children. Patients often present with vague abdominal discomfort/ pain and an enlarging abdominal mass. Not infrequently, patients are asymptomatic and the tumors are found incidentally on physical examination or by imaging for the workup for unrelated conditions.

Jaundice and hormonal disturbances are rare. Ultrasound and computed tomography (CT) usually reveal a well-demarcated and variably cystic mass, averaging 10 cm and usually located in the body or tail of the pancreas. Tumor calci? cation may be present. As smaller tumors are identi? ed with the increased use of more sensitive imaging techniques, cystic degeneration and calci? - cation are often not seen.

General Diagnostic Approach

Solid-pseudopapillary neoplasms (SPPNs) may appear either primarily solid or cystic radiologically and, as a result, one may start at different points within our algorithms. Unlike true cystic neoplasms of the pancreas, aspirates from the lesions are almost always cellular. Because the neoplastic cells of SPPN appear monotonous and less cohesive when compared to pancreatic ductal adenocarcinomas (PDAs), the cytologist usually has little problem distinguishing the two entities.

However, it can be a challenge to distinguish SPPN from other epithelioid neoplasms, such as pancreatic endocrine tumors (PETs). Because signi? cant overlap of cytologic features is often noted among these lesions and speci? c therapy may depend upon the diagnosis, one should be wary to give a de? nitive diagnosis without ancillary studies. In equivocal cases, one may choose to render a less de? nitive diagnosis such as “epithelioid neoplasm” and discuss the differential diagnosis in a note.

Diagnostic Criteria


Aspirates from these neoplasms are usually cellular and show characteristic cytologic ? ndings (Table 7-1). However, when only cystically degenerated areas are sampled, the smears may rarely be paucicellular and contain predominantly proteinaeous ? uid and/or necrotic debris, which may then result in a false-negative diagnosis. Neoplastic cells are arranged singly, in loosely cohesive clusters and in linear and branching papillary structures."

Erscheint lt. Verlag 5.5.2010
Reihe/Serie Essentials in Cytopathology
Essentials in Cytopathology
Vorwort M.W. Stanley
Zusatzinfo XII, 204 p. 172 illus., 168 illus. in color.
Verlagsort New York
Sprache englisch
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete
Studium 2. Studienabschnitt (Klinik) Pathologie
Schlagworte carcinoma • Cell • cytology • Cytopathology • Lymphoma • pancreas • Tumor
ISBN-10 0-387-68947-8 / 0387689478
ISBN-13 978-0-387-68947-0 / 9780387689470
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