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Radiology Illustrated_ Chest Radiology ( PDFDrive ).pdf
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198 20 Ground-Glass Opacity with Reticulation

Key Points for Differential Diagnosis

 

Distribution

 

 

 

 

 

 

 

Zones

 

 

 

 

 

Clinical presentations

 

Diseases

U

M

L

SP

C R BV

R

Acute Subacute Chronic

Others

Pneumocystis

+

+

+

 

+

 

+

+

 

pneumonia

 

 

 

 

 

 

 

 

 

AIP or ARDS

+

+

+

 

+

 

+

+

 

DAD superimposed

 

+

+

+

 

 

 

+

Acute exacerbation of UIP

on UIP

 

 

 

 

 

 

 

 

 

DAH

+

+

+

 

+

 

+

+

Subpleural (apical and costophrenic angle) sparing

PE

 

+

+

 

+

 

+

+

 

PAP

+

+

+

 

+

 

+

+

 

NSIP

 

+

+

+

+

+

+

+

 

Subacute HP

+

+

 

 

+

 

+

+

 

OP

 

+

+

+

 

+

 

+

 

Sarcoidosis

+

+

 

 

+

+

 

+

 

LP

 

+

+

 

+

 

+

+

 

Mucinous AD

+

+

+

 

+

 

+

+

 

Note: AIP acute interstitial pneumonia, ARDS adult respiratory distress syndrome, DAD diffuse alveolar damage, UIP usual interstitial pneumonia, DAH diffuse alveolar hemorrhage, PE pulmonary edema, PAP pulmonary alveolar proteinosis, NSIP nonspeciÞc interstitial pneumonia, HP hypersensitivity pneumonitis, OP organizing pneumonia, LP lipoid pneumonia, AD adenocarcinoma, U upper, M middle, L lower, SP subpleural, C central, R random, BV bronchovascular

Pneumocystis jirovecii Pneumonia

Pathology and Pathogenesis

The alveoli are Þlled by a foamy, pale, and eosinophilic exudate (Fig. 20.6). The fungus is unstained in Hematoxylin and Eosin preparations but with silver stain the alveoli are seen to contain numerous round cysts that measure about 5 μm across. Crescent-shaped forms represent collapsed cysts. Other helpful feature is a dot, generally seen on the edge of the cyst. In bronchoalveolar lavage ßuids, frothy exudate is frequently seen and it may be a diagnostic tool if a biopsy cannot be studied [9].

Symptoms and Signs

Pneumocystis jirovecii pneumonia can occur in immunocompromised individuals, especially hematopoietic stem and solid organ transplants, those receiving high-dose corticosteroid therapy, and persons with advanced HIV infection [10]. A slow indolent time course with symptoms of pneumonia progressing over weeks to months is characteristic in HIV-infected patients. Fulminant respiratory failure associated with fever and dry cough is typical in non-HIV-infected patients.

CT Findings

Thin-section CT (TSCT) typically shows bilateral areas of GGO [11] (Fig. 20.6). The areas of GGO may be patchy, have a geographic appearance, be diffuse, or involve mainly the perihilar regions or upper lobes. Reticulation or interlobular septal thickening is seen in approximately 20 % of patients forming Òcrazy-paving appearanceÓ (Fig. 20.6). Cyst formation is seen in about 30 % of patients. The cysts are variable in appearance, but most measure 5Ð30 mm in diameter, are thin walled, and are located in the upper lobes. Unusual manifestations include nodules and a miliary pattern [12].

CT–Pathology Comparisons

The GGO reßects thickening of alveolar wall by edema or interstitial pneumonitis and foamy nature of alveolar exudates, whereas the reticulation reßects the organization of intra-alveolar materials or Þbrosis [8].

Patient Prognosis

The Þrst-line drug for treatment and prevention is trimethoprimÐsulfamethoxazole. To reduce the incidence of