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REVIEW

CURRENT
OPINION Necrotizing pneumonia: a rare complication of
pneumonia requiring special consideration
Yueh-Feng Tsai a and Yee-Huang Ku b

Purpose of review
Necrotizing pneumonia is a rare complication of bacterial lung infection. Its cause is owing to either a
virulence factor of the microorganism or a predisposing factor of the host. This disease may cause
devastating complications such as diffuse pulmonary inflammation, septic shock, and respiratory failure,
making treatment more difficult. In the recent decade, the cause of necrotizing pneumonia and the role of
surgical treatment have raised considerable attention, leading to therapeutically specific suggestions.
Recent findings
Staphylococcus aureus strains that produce Panton–Valentine leukocidin have been reported to cause
rapidly progressive necrosis of the lung tissue in young immunocompetent patients. Furthermore, recent
studies have showed the risk of disease progression is associated with underlying medical conditions.
Although antibiotics are the first choice of treatment for necrotizing pneumonia, it has been emphasized
that surgical treatment is a feasible alternative option in patients who fail to respond to antibiotics and
develop continued deterioration and complications.
Summary
The current knowledge of cause, clinical features, diagnosis, treatment, and prognosis of necrotizing
pneumonia are summarized. Antibiotics remain the mainstay of treatment. Lung resection can be
considered an alternative treatment option in patients who are unresponsive to antibiotic therapy and
develop parenchymal complications. Outcome is affected by the degree of disease progression and
comorbidities.
Keywords
bronchopulmonary fistula, lung resection, necrotizing pneumonia, pneumonia, pulmonary infection

INTRODUCTION the development of bronchopleural fistula, life-


A small number of patients with bacterial lung threatening hemoptysis, septicemia, and respiratory
infection do not follow the usual predictable course failure. Surgical treatment has been considered life-
&&

and develop a necrotic process even with optimal saving in these cases [3 ,4,5].
medical treatment. The process is usually rapidly Articles in the literature describe the predispos-
progressive and these patients tend to present with ing risk factors and surgical outcome of necrotizing
&& &&

acute respiratory distress. The affected extent may pneumonia [1,3 ,6 ,7]. This review summarizes
be patchy, segmental, lobar, or even an entire lung the current knowledge of cause, clinical charac-
[1]. Necrotizing pneumonia has been characterized teristics, diagnosis, treatment, and prognosis of
by the finding of pneumonic consolidation with necrotizing pneumonia. Surgical indications and
multiple necrosis of the lung parenchyma. These
necrotic foci may coalesce, resulting in a lung a
Department of Surgery, St. Martin De Porres Hospital, Chiayi and
abscess if localized, or pulmonary gangrene if b
Department of Medicine, Chi Mei Medical Center, Liouying, Tainan,
involving an entire lobe [2]. Taiwan
Treatment of necrotizing pneumonia consists of Correspondence to Yee-Huang Ku, Department of Medicine, Chi Mei
prolonged courses of antibiotics. However, massive Hospital, Liouying, No. 201, Taikang, Liouying District, Tainan City 736,
necrotic tissue makes it difficult for the antibiotics to Taiwan (R.O.C). Tel: +886 6 6226999/77604; fax: +886 6 6226999/
reach the infected areas, as well as leading to the 77610; e-mail: althrisas@gmail.com
progressive destruction and persistent infection of Curr Opin Pulm Med 2012, 18:246–252
the pulmonary parenchyma, possibly followed by DOI:10.1097/MCP.0b013e3283521022

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Necrotizing pneumonia Tsai and Ku

following the introduction of the 7-valent pneumo-


KEY POINTS coccal conjugate vaccine (PCV-7) in 2000 [8,16–19].
 The most common pathogens associated with It has been hypothesized that S. pneumoniae serotype
necrotizing pneumonia are Staphylococcus aureus, 3 leading to necrosis is probably related to the
Streptococcus pneumoniae, and Klebsiella pneumoniae. inflammatory response to the capsular polysacchar-
ides and its ability to resist phagocytosis [8]. In
 Patients developing necrotizing pneumonia usually
addition, other nonvaccine S. pneumoniae serotypes
have concomitant medical illness, the most common
being diabetes mellitus and alcohol abuse. have also been reported in the post-PCV-7 era, such
as 1, 14, 15, 19A, and 33 [8,19]. Other streptococci
 Contrast-enhanced chest computed tomography is the that have been reported include b-hemolytic strep-
standard procedure for the diagnosis of necrotizing tococci such as group A streptococci and Streptococ-
pneumonia and is helpful in evaluating the
cus viridans. Group A streptococci are notorious for
parenchymal complications.
invasive infection and childhood pneumonia, and
 Pulmonary resection is a feasible treatment option in are well known to be preceded by a varicella infec-
patients who have no response to antibiotic therapy tion [20,21]. It has been suggested that M protein, a
and develop parenchymal complications such as virulence factor associated with tissue necrosis, con-
persistent pulmonary sepsis, bronchopleural fistula,
tributes to intravascular thrombosis and rapid tissue
hemoptysis, and necrotic parenchyma that is associated
with impaired respiratory function. destruction [10]. S. viridans are frequently isolated in
patients with underlying immune suppression and
 Outcome depends on the degree of disease comorbidities such as corticosteroid therapy and
progression and underlying medical conditions. alcoholism [3 ].
&&

K. pneumoniae has long been documented as the


principal cause of pneumonia. Patients in extreme
age groups and with compromised immune status
techniques with particular attention to lung resec- such as in diabetes mellitus and alcoholism are
tion for necrotic parenchyma are highlighted in susceptible infection. Recent studies report that var-
this article. ious virulence factors, including hypermucoviscos-
ity, K1/K2 capsular serotype, and other virulence-
associated genes, contribute to the pathogenesis of
CAUSE K. pneumoniae infection [22,23,24 ].
&

Although the pathogenesis of necrotizing pneumo- Other identified organisms were Staphylococcus
nia is not clearly defined, most studies believe that epidermidis, Escherichia coli, Acinetobacter baumannii,
tissue necrosis occurs as a result of inflammatory Haemophilus influenzae and Pseudomonas aeruginosa
&&
response due to the toxins produced by the invasive [1,3 ,25]. P. aeruginosa pneumonia is not common
pathogen or the associated vasculitis and venous in healthy persons but usually presents with a ful-
&&
thrombosis [6 ,8–11]. The most common patho- minant and lethal course [25]. It is well recognized
gens are Staphylococcus aureus, Streptococcus pneumo- to invade blood vessels and cause a thrombotic
&& &&
niae, and Klebsiella pneumoniae [1,3 ,6 ,7,12,13]. endarteritis, therefore leading to tissue necrosis
S. aureus is responsible for about 2% of cases [7]. Rarely, anaerobes such as Clostridia species
of community-acquired pneumonia [9]. S. aureus and Bacteroides species are reported. They are
strains, often methicillin-resistant, that produce thought to play a synergistic role in causing necrot-
cytotoxin Panton–Valentine leukocidin (PVL) are izing pneumonia, which is usually a delayed process
associated with causing progressive and hemorrha- [26].
gic necrotizing pneumonia especially in young
&&
immunocompetent patients [9,11,14 ]. Although
most studies reported that PVL served as the CLINICAL FEATURES
mediator of tissue necrosis [9,11], other studies Necrotizing pneumonia tends to occur in adult
also suggested that a-hemolysin and possibly other males with concomitant medical illness such as
cytotoxins are responsible for the pathogenesis of diabetes mellitus, alcohol abuse, and corticosteroid
&& &&
pulmonary disease [15]. therapy [3 ,14 ]. In contrast, the pediatric patients
Streptococci are considered important patho- are predominantly composed of healthy female
&&
gens too. S. pneumoniae is the most common cause children [6 ,13,19,20]. Common presenting symp-
of bacterial pneumonia in children and an increase toms include fever, cough, chest pain, and shortness
&& &&
in necrotizing pneumonia has been observed since of breath [4,6 ,14 ]. These patients may have
1990 [8,13,16,17]. Nonvaccine S. pneumoniae purulent sputum and sometimes present with
serotype 3 has become a significant contributor confusion [27,28]. Duration of symptoms prior to

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Infectious diseases

hospitalization is extremely variable, ranging from


several days to 1 week [4,20,27].
Necrotizing pneumonia may associate with high
inflammatory markers such as high levels of white
blood cells, erythrocyte sedimentation rate, and
C-reactive protein. In addition, signs of complicated
clinical prognosis, including longer duration of
symptoms, higher ratio and longer duration of
hospitalization, increased number of febrile days,
longer normalization period of C-reactive protein
levels, and higher cost of treatment are reported [29].
The necrotic process can occur at any lobe of
the lung but involvement of the right lower,
right middle, and left lower lobes is more fre-
&&
quent [1,3 ,13,29]. A parapneumonic effusion or
empyema is a common complication of necrotizing
&&
pneumonia [1,3 ]. The patient’s condition can be
further complicated by the development of high-
output bronchopleural fistula, massive hemoptysis,
&&
and bilateral diffuse pneumonia [1,3 ,12,29]. Septic
shock and respiratory failure may subsequently
occur, leading to the necessity for vasopressor
&&
therapy and ventilator support [3 ,4,20].

FIGURE 1. Consolidation and collapse in the right lung with


DIAGNOSIS a large loculated effusion. This is a 46-year-old-man with
Confirming the etiologic pathogens responsible for diabetes mellitus and alcoholism. Mild left pulmonary
severe, rapidly progressive pneumonia is important infiltrates are noted.
to direct antibiotic treatment. However, a positive
microbiology result is not always obtainable.
Sputum Gram’s stain can be quickly obtained but Contrast-enhanced chest CT is the standard
usually shows large concentrations of Gram-positive procedure in making the diagnosis of necrotizing
and Gram-negative bacteria [7]. The result of spu- pneumonia and is helpful in evaluating the paren-
tum culture is also not reliable owing to contami- chymal complications that are not appreciated on
nation from normal oropharyngeal flora. Cultures chest films. Any delay in confirming the diagnosis is
of peripheral blood (if bacteremia is suspected), probably due to the delay in performing the chest
pleural fluid (when pleural effusion coexists), and CT [29]. When chest radiography shows progressive
infected lung tissue (obtained at the time of surgery) pneumonia, the occurrence of a pleural effusion or
give the most reliable results to establish a bacter- hydropneumothorax, or when patients develop
iologic diagnosis of necrotizing pneumonia. The hemoptysis, respiratory distress or septic shock
overall positive percentage variably ranges between despite appropriate medical treatment, chest CT
&& && &&
40 and 100% [1,3 ,6 ,12,13]. scan should be performed promptly [3 ,13]. Pneu-
The diagnosis of necrotizing pneumonia is made monic consolidation with multiple areas of necrotic
generally according to chest imaging studies, includ- low attenuation on CT is suggestive of necrotizing
&&
ing a series of radiography and contrast-enhanced pneumonia (Fig. 3) [1,3 ,29].
&&
computed tomography (CT) [3 ,13,19]. Early in the Proximal endobronchial obstructing lesions,
disease course, necrotizing pneumonia typically which present with fever, cough, and pulmonary
appears as consolidation on the chest radiograph. consolidation, may mimic the clinical and radio-
Repeated radiographic evaluation every 3–4 days is graphic features of necrotizing pneumonia. These
advocated to determine the effects of antibiotic lesions include a foreign body and endobronchial
therapy and detect the occurrence of complications malignancy. CT can help identify most endobron-
&&
[3 ]. As the disease is associated with empyema or chial foreign bodies. Complete consolidation of a
bronchopleural fistula, a pleural effusion (Fig. 1) or lobe, however, may possibly mask the presence of an
pneumothorax (Fig. 2) can be seen. However, it is underlying carcinoma. Bronchoscopy is useful to
common for chest radiography to underestimate the differentiate necrotizing pneumonia from proximal
degree of parenchymal destruction [1,30]. endobronchial obstruction.

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Necrotizing pneumonia Tsai and Ku

TREATMENT
Treatment of necrotizing pneumonia is primarily
medical. However, when the disease deteriorates
or complications occur in spite of optimal medical
treatment, surgical intervention should be con-
sidered an alternative treatment.

Antibiotics
Intravenous antibiotic therapy remains the main-
stay treatment of necrotizing pneumonia. The
choice of initial antibiotics should be directed at
broad coverage with commonly implicated patho-
gens (S. aureus, streptococci, K. pneumoniae, etc) [7].
Additional empirical anaerobic antibiotic should be
considered in patients with lung abscesses. Once the
causative pathogens and sensitivities are known,
antibiotics can be modified accordingly. However,
the patients’ clinical information and the local
susceptibility pattern of the possible pathogen such
as the incidence of penicillin-nonsusceptible or
ceftriaxone-nonsusceptible Streptococcus pneumoniae
and community-acquired methicillin-resistant
Staphylococcus aureus (MRSA), also determine the
FIGURE 2. Extensive consolidation and collapse with a choice of antibiotics.
pneumothorax in a 78-year-old-woman with corticosteroid Empiric penicillins or ceftriaxone (if penicillin-
therapy. 700 ml of pus was drained and there was persistent nonsusceptible S. pneumoniae was considered) or
air leak. glycopeptide (if ceftriaxone-nonsusceptible S. pneu-
moiae was considered) are recommended. Clinda-
mycin or metronidazole can be used in combination
to cover possibly involved anaerobes. Respiratory
quinolones, such as levofloxacin or moxifloxacin
(which can also cover anaerobic infection), are an
alternative choice especially for those patients aller-
gic to penicillins or cephalosporins. Glycopeptide or
linezolid is recommended in treating community-
&&
acquired MRSA infection [14 ]. Linezolid and clin-
damycin have been reported to have better result
in treating staphylococcal necrotizing pneumonia
&&
as a result of inhibiting PVL production [14 ].
In hospital-acquired infection, antipseudomonas
b-lactams or/and quinolones, or both, are recom-
mended if pseudomonas is considered, and even
carbepenem if a multidrug resistant organism is
considered. If the culture results are negative, the
adjustment of antibiotics may depend on the treat-
ment response of clinical parameters (e.g. symptoms
and signs, inflammatory markers, chest radio-
graphs).

Chest tube drainage


FIGURE 3. Contrast-enhanced chest CT reveals pneumonic Chest tube drainage may be undertaken for symp-
consolidation with multiple areas of necrotic low attenuation tomatic relief in necrotizing pneumonia with large
involving the whole left lower lobe. This is a 56-year-old-man pleural fluid collections or pyopneumothorax. It
with diabetes mellitus. may be technically difficult to insert the chest tube

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Infectious diseases

into the pleural space because an inflammatory tolerate pneumonectomy [1,4,7]. In addition, a con-
pleural adhesion commonly occurs. Even if success- siderable number of patients have pleural collec-
ful, the result of drainage is unsatisfactory, as pleural tions at the time of surgery. Thus, decortication
fluid frequently becomes loculated. Furthermore, should also be undertaken to facilitate expansion
a retrospective study in children showed pleural of the remaining lung.
drainage increased the incidence of ongoing air leak Necrotizing pneumonia often leaves the inter-
through a bronchopleural fistula [31]. lobar fissure densely fused and the involved paren-
chyma tends to become heavy and firm, making
pulmonary resection very difficult. Recent studies
Surgery recommend the key technique is to ligate and sever
Surgical debridement or resection may be con- the pulmonary veins first. This procedure permits
&&
sidered for patients who fail to improve with the lung to be retracted more easily [1,3 ]. When a
medical management. However, the optimal indica- densely fused fissure is encountered, direct dissec-
tions and timing of surgery are unclear. It is recom- tion of the pulmonary artery in the fissure is risky
mended that a surgical approach should be and not suggested. Alternatively, the fissure can be
considered if patients develop continued deteriora- divided between clamps in small steps from both
tion or have complications despite the use of anti- ends but sparing the central area within which the
biotic therapy and less invasive procedures. pulmonary arteries lay. The central fused paren-
Accordingly, the primary indications include per- chyma is further divided vertically by electrocautery
sistent fever and leukocytosis, occurrence of without injuring the artery until a TA 60 stapler
empyema, bronchopleural fistula and hemoptysis, (4.8 mm, green cartridge) can be applied. The
and necrotic parenchyma that is responsible for remaining tissues between the involved and healthy
&& &&
impaired respiratory function [1,3 ,6 ,7,12]. lobes are temporarily clamped with the stapling
Furthermore, for patients with respiratory failure device in atelectasis. The healthy lung is inflated
and septic shock who are stabilized after medical to confirm that the proposed line of transection is
treatment, surgical intervention can be an option if correct. Then the staples are advanced, and the
&&
parenchymal complications occur [1,3 ,7]. On the involved lobe is resected. The resection margin of
contrary, a higher risk of postoperative death and the left lung is reinforced with continuous mono-
&&
ventilator dependency is observed in patients with filament absorbable sutures [3 ]. Several authors
bilateral diffuse disease and preexisting organ failure advocated covering the bronchial stump with tissue
such as liver cirrhosis, renal failure, and chronic flaps to reduce the risk of stump leak, particularly
&&
obstructive pulmonary disease [1,3 ,7]. Extensive after pneumonectomy [1,7,12]. However, a recent
lung resection should be avoided in such cases. investigation with 26 patients undergoing pulmon-
The operation can be performed with single- ary resection for necrotizing pneumonia showed
lung anesthesia using a double-lumen endobron- lobectomies and bilobectomies can be safely per-
&&
chial tube to facilitate exposure. To prevent the formed without the use of a flap [3 ].
spread of secretions to the contralateral lung, the The main postoperative complications include
airway must be frequently suctioned during surgical persistent air leak, empyema, and ventilator
manipulation. Patients may not tolerate one-lung dependency. A recent publication with 20 children
ventilation, which increases the surgical difficulty. reported that postoperative persistent air leak
Alternative use of one-lung and two-lung venti- occurred in 20% of patients, all of whom received
&&
lation is a way to maintain adequate saturation of segmentectomy [6 ]. Prolonged chest tube drainage
&&
oxygen during the whole course of surgery [3 ]. is required in these cases and the chest tube ulti-
The type of surgical resection is based on the mately can be safely removed as a result of post-
extent of the pulmonary necrosis and is always as operative pleural symphysis. A residual space after
conservative as possible. If the necrotic parenchyma lobectomy or pneumonectomy may increase the
is confined to the periphery, it can be treated by risk of postoperative empyema. A pleural irrigation
debridement, wedge resection, or segmentectomy. system or obliteration of the space with a muscle
When the affected parenchyma is too extensive to flap seems to reduce the incidence of postoperative
completely remove the infected tissue using partial pleural infection [1,7]. Once this complication
resection of a lobe, lobectomy is indicated occurs, it is usually localized and can be managed
&& && &&
[1,3 ,6 ]. The necrotizing process can possibly by percutaneous drainage [3 ,12]. Patients with
involve multiple lobes. A significantly more invasive bilateral diffuse disease tend to become ventilator
procedure such as bilobectomy and pneumonec- dependent following lung resection [1]. Debride-
tomy may be required. Literature demonstrates that ment of necrotic parenchyma is an alternative
patients with unilateral involvement can well approach [7].

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Necrotizing pneumonia Tsai and Ku

3. Tsai YF, Tsai YT, Ku YH. Surgical treatment of 26 patients with necrotizing
PROGNOSIS && pneumona. Eur Surg Res 2011; 47:13–18.
The mortality of necrotizing pneumonia is difficult In this study, authors describe the common comorbidities and complications of
necrotizing pneumonia. They also highlight the indications and techniques of
to assess because of its rarity, but is likely to be high. surgical resection for necrotic lung tissue and conclude that pulmonary resection
There are also not enough data to compare the is a feasible treatment option for patients who have no response to antibiotic
therapy and develop parenchymal complications.
results of surgical resection with medical therapy 4. Chen CH, Huang WC, Chen TY, et al. Massive necrotizing pneumonia with
alone because it is not possible to select those pulmonary gangrene. Ann Thorac Surg 2009; 87:310–311.
5. Evans B, Mackenzie I, Malata C, Coonar A. Successful salvage right upper
patients with a poor prognosis who may benefit lobectomy and flap repair of trachea-esophageal fistula due to severe
from earlier surgical treatment. The survival rate necrotizing pneumonia. Interact Cardiovasc Thorac Surg 2009; 9:896–
898.
of lung resection for necrotizing pneumonia refrac- 6. Westphal FL, Lima LC, Lima Netto JC, et al. Surgical treatment of children with
tory to medical therapy ranges between 80 and 95% && necrotizing pneumonia. J Bras Pneumol 2010; 36:716–723.
&& &&
Authors emphasize chest CT should be performed in pneumonia children with
[1,3 ,6 ,7,29]. Bilateral diffuse disease and preex- persistent fever, worsening of clinical status, or pleural complications despite
isting organ failure appear to be important predic- appropriate antibiotic therapy. They advocate surgical resection is indicated in
&&
cases of septicemia, bronchopleural fistula, or acute respiratory failure that are
tors of surgical outcome [1,3 ,7]. Moreover, Li et al. refractory to medical treatment.
&&
[14 ] suggest that necrotizing pneumonia due to S. 7. Karmy-Jones R, Vallières E, Harrington R. Surgical management of necrotizing
pneumonia. Clin Pulm Med 2003; 10:17–25.
aureus has a worse prognosis when flu-like symp- 8. Hsieh YC, Hsueh PR, Lu CY, et al. Clinical manifestations and molecular
toms, hemoptysis, and leukopenia are present. epidemiology of necrotizing pneumonia and empyema caused by Strepto-
coccus pneumoniae in children in Taiwan. Clin Infect Dis 2004; 38:830–
835.
9. Gillet Y, Issartel B, Vanhems P, et al. Association between Staphylococcus
aureus strains carrying gene for Panton-Valentine leukocidin and highly lethal
CONCLUSION necrotising pneumonia in young immunocompetent patients. Lancet 2002;
Antibiotics remain the mainstay of treatment for 359:753–759.
10. Bryany AE. Biology and pathogenesis of thrombosis and procoagulant activity
necrotizing pneumonia. Once patients have contin- in invasive infections caused by group A streptococci and Clostridium
ued deterioration or develop associated compli- perfringens. Clin Microbiol Rev 2003; 16:451–462.
11. Labandeira-Rey M, Couzon F, Boisset S, et al. Staphylococcus aureus
cations despite appropriate antibiotic therapy, Panton–Valentine leukocidin causes necrotizing pneumonia. Science
contrast-enhanced CT must be performed promptly 2007; 315:1130–1133.
12. Krishnadasan B, Sherbin VL, Vallières E, Karmy-Jones R. Surgical manage-
to confirm the diagnosis of necrotizing pneumonia ment of lung gangrene. Can Respir J 2000; 7:401–404.
and evaluate the extent of involvement. Pulmonary 13. Chen KC, Su YT, Lin WL, et al. Clinical analysis of necrotizing pneumonia in
children: three-year experience in a single medical center. Acta Paediatr Tw
resection is reserved for patients who have no 2003; 44:343–348.
response to antibiotic therapy and develop paren- 14. Li HT, Zhang TT, Huang J, et al. Factors associated with the outcome of life-
&& threatening necrotizing pneumonia due to community-acquired Staphylococ-
chymal complications. Outcome is affected by the cus aureus in adult and adolescent patients. Respiration 2011; 81:448–460.
degree of disease progression and underlying In this study, authors performed a literature review and concluded necrotizing
pneumonia due to S. aureus has a worse prognosis when flu-like symptoms,
medical conditions. Further studies to determine hemoptysis, and leukopenia are present. They proposed the use of antibiotics such
the mechanism of pulmonary necrosis are needed. as linezolid and clindamycin, which inhibit PVL production, is a more appropriate
treatment for staphylococcal necrotizing pneumonia.
In addition, because necrotizing pneumonia is rare 15. Ho PL, Cheng VC, Chu CM. Antibiotic resistance in community-acquired
and because the precise indications of lung resection pneumonia caused by Streptococcus pneumoniae, methicillin-resistant
Staphylococcus aureus, and Acinetobacter baumannii. Chest 2009; 136:
remain unclear, large-scale, randomized controlled 1119–1127.
trials are required to guide treatment and define the 16. Bender JM, Ampofo K, Korgenski K, et al. Pneumococcal necrotizing pneu-
monia in Utah: dose serotype matter? Clin Infect Dis 2008; 46:1346–1352.
requirement for pulmonary resection. 17. Tan TQ, Mason EO Jr, Wald ER, et al. Clinical characteristics of children with
complicated pneumonia caused by Streptococcus pneumonia. Pediatrics
2002; 110:1–6.
Acknowledgements 18. American Academy of Pediatrics. Committee on Infectious Diseases. Policy
statement: recommendations for the prevention of pneumococcal infections,
None. including the use of pneumococcal conjugate vaccine (Prevnar), pneumo-
coccal polysaccharide vaccine, and antibiotic prophylaxis. Pediatrics 2000;
106:362–366.
Conflicts of interest 19. Hsieh YC, Hsiao CH, Tsao PN, et al. Necrotizing pneumococcal pneumonia in
There are no conflicts of interest. children: the role of pulmonary gangrene. Pediatr Pulmonol 2006; 41:623–
629.
20. Cengiz AB, Kanra G, Caĝlar M, et al. Fatal necrotizing pneumonia caused by
group A streptococcus. J Paediatr Child Health 2004; 40:69–71.
21. Stride PJ, Campher MJ, Geary JM, et al. Adult chicken pox complicated by
REFERENCES AND RECOMMENDED fatal necrotizing pneumonia. Med J Aust 2004; 181:160–161.
READING 22. Ku YH, Chuang YC, Yu WL. Clinical spectrum and molecular characteristics
Papers of particular interest, published within the annual period of review, have of Klebsiella pneumoniae causing community-acquired extrahepatic abscess.
been highlighted as: J Microbiol Immunol Infect 2008; 41:311–317.
& of special interest 23. Okada F, Ando Y, Honda K, et al. Acute Klebsiella pneumoniae pneumonia
&& of outstanding interest alone and with concurrent infection: comparison of clinical and thin-section
Additional references related to this topic can also be found in the Current CT findings. Br J Radiol 2010; 83:854–860.
World Literature section in this issue (p. 285). 24. Lin YC, Lu MC, Tang HC, et al. Assessment of hypermucoviscosity as a
& virulence factor for experimental Klebsiella pneumoniae infections: compara-
1. Reimel BA, Krishnadasen B, Cuschieri J, et al. Surgical management of acute tive virulence analysis with hypermucoviscosity-negative strain. BMC Micro-
necrotizing lung infections. Can Respir J 2006; 13:369–373. biol 2011; 11:50–58.
2. Chapman SJ, Lee YCG, Davies RJ. Respiratory infections. 1st ed. In: This article proposed that other virulent factors apart from hyperviscosity may be
Torres A, Ewig S, Mandell L, Woodhead M. (editors). Empyema, lung responsible for pyogenic K. pnemoniae infection.
abscess, and necrotizing pneumonia. London: Edward Arnold; 2006. 25. Crnich CJ, Gordon B, Andes D. Hot tub-associated necrotizing pneumonia
pp. 385–397. due to Pseudomonas aeruginosa. Clin Infect Dis 2003; 36:e55–e57.

1070-5287 ß 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins www.co-pulmonarymedicine.com 251

Copyright © Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited.
Infectious diseases

26. Cannon JW. Necrotizing clostridial pneumonia: a case report and review of 29. Hacimustafaoglu M, Celebi S, Sarimehmet H, et al. Necrotizing pneumonia in
the literature. Mil Med 2002; 167:85–86. children. Acta Paediatr 2004; 93:1172–1177.
27. Tseng MU, Wei BH, Lin WJ, et al. Fetal sepsis and necrotizing pneumonia in a 30. Wong KS, Chiu CH, Yeow KM, et al. Necrotizing pneumonitis in children. Eur J
child due to community-acquired methicillin-resistant Staphylococcus aureus: Pediatr 2000; 159:684–688.
case report and literature review. Scand J Infect Dis 2005; 37:504–537. 31. Hoffer FA, Bloom DA, Colin AA, Fishman SJ. Lung abscess versus necrotizing
28. Al-Saleh S, Grasemann H, Cox P. Necrotizing pneumonia complicated by pneumonia: implications for interventional therapy. Pediatr Radiol 1999;
early and late pneumatoceles. Can Respir J 2008; 15:129–132. 29:87–91.

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