Contents
Download PDF
pdf Download XML
44 Views
6 Downloads
Share this article
Research Article | Volume 15 Issue 3 (March, 2025) | Pages 146 - 151
Evaluating the role of the Fournier's Gangrene Severity Index in predicting patient outcomes
 ,
 ,
 ,
 ,
1
Assistant Professor, Dept of General Surgery, Katuri medical college and Hospital, Guntur.
2
Associate Professor, Dept of General Surgery, Katuri Medical College and Hospital, Guntur.
3
Postgraduate in Department of General Surgery, Katuri Medical College and Hospital
Under a Creative Commons license
Open Access
Received
Feb. 2, 2025
Revised
Feb. 16, 2025
Accepted
Feb. 26, 2025
Published
March 7, 2025
Abstract

Background: Fournier's gangrene is a severe form of necrotizing fasciitis of the perineum and genitalia, typically caused by a polymicrobial infection.Most individuals with Fournier's gangrene also associated with comorbid conditions, such as diabetes, alcoholism, and other related disorders.The Fournier’s Gangrene Severity Index (FGSI) is a valuable prognostic tool for predicting mortality and survival outcomes in patients with Fournier’s gangrene. Reconstructive interventions are required when significant tissue defects arise from extensive tissue damage. AIM:To study the etiology, microbiological factors and reconstructive procedures performed in patients with Fournier’s gangrene, and to assess the outcomes and mortality rates of Fournier’s gangrene based on the Fournier’s Gangrene Severity Index (FGSI). Results:Among 40 patients treated at KMCH from May 2022 to May 2024. Most commonly occurred in the fourth and fifth decades of life, with a mean age of 50.2 years. The mean age for deceased patients was 63 years, significantly higher than the 48.3 years among survivors. The male-to-female ratio was 34:6.The most common source of infection was genitourinary (40%), followed by anorectal (27.5%) and 20% of cases being idiopathic. Diabetes mellitus (47.5%) was the most prevalent comorbidity, followed by chronic alcoholism (22.5%) and HIV (10%). Polymicrobial infections were seen in 80% of cases, with E. coli (47%),streptococci (41.1%), and Klebsiella (35.3%) being the most frequently isolated pathogens. Bacteroides were the most common anaerobes (8.9%). In most cases, the infection was confined to the genitalia (52.9%). The Fournier’s Gangrene Severity Index (FGSI) was a reliable predictor of survival, with a score above 10.5 associated with 100% mortality, while a score below 10.5 correlated with 93.3% survival. Conclusion: Fournier’s gangrene (FG) predominantly affects middle-aged and elderly males, with genitourinary infections as the most common source. Diabetes mellitus is the leading comorbidity, and infections are typically polymicrobial. Early diagnosis, repeated debridement, and reconstructive procedures for tissue loss are essential for improving survival outcomes. Despite aggressive treatment, mortality remains significant. The Fournier’s Gangrene Severity Index (FGSI) is a key predictor of survival, with higher scores correlating to increased mortality

Keywords
INTRODUCTION

Fournier's gangrene is a severe form of necrotizing fasciitis of the perineum and genitalia, typically caused by a polymicrobial infection. Most individuals with Fournier's gangrene also associated with comorbid conditions, such as diabetes, alcoholism, and other related disorders.

 

The Fournier’s Gangrene Severity Index (FGSI) is a valuable prognostic tool for predicting mortality and survival outcomes in patients with Fournier’s gangrene. Reconstructive interventions are required when significant tissue defects arise from extensive tissue damage.

 

AIM:

  • To study the etiology and microbiological factors associated with Fournier’s gangrene.
  • To study the reconstructive procedures performed in patients with Fournier’s gangrene.
  • To evaluate the outcomes of Fournier’s gangrene based on the Fournier’s Gangrene Severity Index (FGSI).
  • To assess the mortality rates associated with Fournier’s gangrene in relation to the FGSI.
MATERIALS AND METHODS

Study area: Katuri medical college and hospital, (KMCH) Guntur.

Study period: May 2022 to April 2024

 

Study population Patients presenting to the outpatient department and emergency department of KMCH.

 

OBJECTIVES OF THE STUDY:

  1. To analyze the various etiological and predisposing factors contributing to the development of Fournier’s gangrene.
  2. To analyse the progression of Fournier’s gangrene in relation to the timing of patient presentation.
  3. To evaluate the outcomes of Fournier’s gangrene based on the Fournier’s Gangrene Severity Index (FGSI).

Inclusion criteria:

Patients presenting with gangrene of genitalia and perineum

- Age more than 12 years

 

Exclusion criteria:

- Age less than 12 years.

 

Sample size: 40.

All patients eligible by inclusion and exclusion criteria were included in the study.

 

RESULTS

This study includes a total of 40 cases that were studied prospectively over a period of two years that were treated as inpatient basis at KMC&H from May 2022 to April 2024.

 

INCIDENCE SEX WISE:

Sex

Number

Percentage

Male

34

85

Female

6

15

 

INCIDENCE AGEWISE:

Age group in years

Number of patients

Percentage of patients

Below 30

0

0

31-40

5

12.5

41-50

15

37.5

51-60

8

20

61-70

7

17.5

71-80

5

12.5

>80

0

0

 

CAUSATIVE FACTORS:

Source of the disease

Number of patients

Percentage of patients

Anorectal

11

27.5

Genitourinary

16

40

Dermatological

5

12.5

Idiopathic

8

20

 

COMORBID FACTORS:

Comorbid conditions

Number of patients

Percentage of patients

Present

33

82.5

Absent

7

17.5

 

MICROBES ISOLATED:

Number of microbes isolated

Number of cases

Percentage of cases

Nil

1

2.5

One

7

17.5

Two

22

55

Three

6

15

Four

4

10

 

Polymicrobial presentation – 80%

Average number of isolates per culture- 2.12

 

In percentage of isolated organisms. E. coli was the most common (47.0%), followed by Streptococcus (41.1%), Klebsiella (35.3%), and Pseudomonas (26.5%). Other organisms included Staphylococcus (17.7%), Enterococcus and Proteus (11.8% each), Bacteroides (8.9%), and Acinetobacter (5.9%)

 

EXTENT OF INVOLVEMENT:

Extent of involvement

Number of cases

Percentage of cases

Limited to the genitalia

21

52.5

Involving the genitalia and perineum

15

37.5

Extending to abdominal wall and proximal thighs

4

10

 

NUMBER OF DEBRIDEMENTS REQUIRED:

Number of debridement’s done

Number of cases

Percentage of cases

One

9

22.5

Two

11

27.5

Three

10

25

Four

5

12.5

Five

4

10

Six

0

0

Seven

1

2.5

 

PATIENTS REQUIRING RECONSTRICTIVE PROCEDURES

Reconstruction done

Number of cases

Percentage of cases

Yes

17

42.5

No

23

57.5

 

TYPES OF RECONSTRUCTIVE PROCEDURES NEEDED:

No Reconstructive procedures performed

Number of cases

Percentage of cases

Primary closure

13

32.5

Local skin flap

2

5

SSG + primary closure

1

2.5

SSG + implantation of testis in thigh

1

2.5

 

MORTALITY:

Mortality

Number of cases

Percentage of cases

Yes

6

15

No

34

85

 

FGSI SCORES:

FGSI scores

Number of cases

Score One

1

Score Two

3

Score Three

6

Score Four

6

Score Five

4

Score Six

6

Score Seven

6

Score Eight

2

Score Nine

1

Score Ten

2

Score Eleven

1

Score Twelve

2

 

FGSI SCORE IN NON – SURVIVOURS:

Non-survivor patient number

FGSI score

Patient one

11

Patient two

8

Patient three

9

Patient four

12

Patient five

10

Patient six

12

 

FGSI SCORE IN SURVIVORS:

FGSI SCORE

Number of cases

Score one

1

Score two

3

Score three

6

Score four

6

Score five

4

Score six

6

Score seven

2

Score eight

5

Score ten

1

DISCUSSION

SEXWISE INCIDENCE

In a large series conducted male to female ratio was 10: 1 (Eke, 2000)1. The following is the list of male to female ratio in the various studies conducted. As per Basoglu et al., 20072 study the M:F ratio was 44:1, as per Baek et al., 20033 study M:F ratio was 14:2, as per Kim KM et al., 20104study M:F ratio was25:2, as per Villlanueva-Saenz et al., 20025 study M:F ratio was 28:0, in present study M:F ratio was 34:6, significant female involvement.

 

Study

Male : female

Basoglu et al., 20072

44 :1

Baek et al., 20033

14 : 2

Kim KM et al., 20104

25: 2

Villlanueva-Saenz et al., 20025

28: 0

Present series

34:6

 

AGEWISE INCIDENCE:

The average age of incidence in 1945 was 40.9 years. In many studies conducted at present it usually ranges from 50 to 70 years. The following is the list of age wise incidence in a few conducted studies. As per Basoglu et al., 20072 clinical study the mean age was 54.0, as per Kim KM et al., 20104 clinical study the mean age was 52.8, as per Yeniyol et al., 20046 clinical study mean age was 51.7, as per Korkut et al., 20037 clinical study mean age was 54.6, In our present study the mean age was 50.2 which was almost similar to the previous studies.

 

Study

Mean age ( years )

Basoglu et al., 20072

54.0

Kim KM et al., 20104

52.8

Yeniyol et al., 20046

51.7

Korkut et al., 20037

54.6

Present series

50.2

 

ORIGIN OF INFECTION:

In a large studies from Eke et al., 20008 the source of infection was 21% anorectal, 19% urological, 24% dermatological and idiopathic in the remaining 34% of cases.

 

In present study the source of infection is 35.3% anorectal, 20.6% urological, 14.7% dermatological and idiopathic in the remaining 29.4% of cases.

 

Anorectal origin is most common source according to Brunet et al.,20009 – 34% and El Mejjad et al.,200210 – 42%, which was similar to the present study.

 

The following is the comparison of present study with Corcoran et al., 200811clinical study shows anorectal origin 38.2% and urogenital origin 11.8%, where as in present study

Anorectal origin is 35.3%, and urogenital origin is 20.6%.

 

Study

Anorectal origin (%)

Urogenital origin (%)

Corcoran et al.,200811

38.2

11.8

Present study

35.3

20.6

 

Study

Anorectal origin (%)

Brunet et al.,20009

34%

El Mejjad et al., 200210

42%

Present study

35.3%

 

COMORBID CONDITIONS:                             

Diabetes mellitus

Diabetes mellitus is known to be associated in 20 – 70% of patients Fournier’s gangrene (Morpurgo, 2002)12. As per Laor et al., 1995 clinical study 30%, and as per Yanar H et al., 2006 clinical study 45.7%, as per Basoglu et al., 2007 clinical study 24.4%, as per Kim KM et al., 2010 clinical study 29.6%, in comparision with multiple studies, present study 36.2% was associated with DM, which is significantly similar with the previous studies.

Study

DM (%)

Laor et al., 1995

30

Yanar H et al., 2006

45.7

Basoglu et al., 2007

24.4

Kim KM et al., 2010

29.6

Present series

36.2

 

Chronic alcoholism

Chronic alcoholism is associated with 25 – 50% of cases with Fournier’s gangrene (Clayton et al., 1990)13. In few studies it is found to be most common comorbid condition (Smith et al., 1998)14.

 

In present study chronic alcoholism is identified as a comorbid condition in 20.6% of case.

 

Microbiology

(Kuzaka B et al.,201815) clinical study reported E coli, streptococcus and Bacteroides and (Smith et al .,1998)14 clinical study reported E coli, streptococcus and Bacteroides as the most commonly isolated microbes. Proud D et al., 201416 proposed that most common organisms were E coli and streptococcus. According to them staphylococcus and enterococcus were commonly isolated more than Bacteroides.

 

It is postulated that, anaerobes even when present are less frequently isolated because of difficulty in preserving samples

In the present series E coli (47.0%) and streptococcus (41.1%) are the most commonly isolatedaerobes.Bacteroides are most commonly isolated anaerobes (8.9%).

 

(lewis et al., 202117)reported polymicrobial isolation in 90% of cases and no growth in 5% of patients. Ferreira et al.,200718 reported polymicrobial growth in 82.9% of cases. In the present study polymicrobial isolation is found in 79.4% of cases and no growth reported in 5.9% of patients.

 

According to (proud D et al) mean microbial number of 2 was identified in culture tests. According to (thwaini et al., 2006) mean number of isolates are approximately 3.In present study the average number of isolates found per case are 2.12.

 

 

Study

Polymicrobial organisms

kuzuka et al., 201815

E coli, streptococcus & Bacteroides

Smith et al ., 1998 14

E coli, streptococcus & Bacteroides

proud et al., 2014 16

E coli, streptococcus

Present series

E coli, streptococcus

 

Study

Polymicrobial %

Lewis et al 202117

90%

Ferreira et al 2007 18

82.9%

Present series

79.4%

 

 

Study

Mean microbial number

proud et al16

2

thwaini et al 19

3

Present series

2.12

 

Extent of involvement

Ferrira et al., 200718 proposed that scrotal involvement found in 93.3% of cases and perineal involvement in 37.2% of cases. Anterior abdominal wall involvement 5.6%.

 

In the present series genital involvement is noted in 100% of cases, perineal involvement in 47.1% of cases and anterior abdominal wall involvement in 11.8% of cases. In the present study all cases have genital involvement irrespective of gender

 

Study

Ferrira et al18

Present series

Scrotal involvement

93.3%

100%

Scrotum and perineal involvement

37.2%

47.1%

Abdominal wall involvement

5.6%

11.8%

 

MANAGEMENT:

Imaging could not be performed uniformly across all patients due to late presentation with extensive disease. Broad-spectrum antibiotics covering gram-positive organisms, gram-negative organisms, and anaerobes were empirically initiated and adjusted based on culture and sensitivity results. Comorbidities and complications were managed accordingly, and patients underwent multiple wound debridement’s.

 

Topical hydrogen peroxide was applied to all patients, showing positive outcomes with repeated debridement’s and daily dressings.

 

Per-urethral catheterization was performed in all cases. Suprapubic catheterization, colostomy, and rectal diversion were not used. Orchidectomy and penectomy were not needed, as there was no involvement of the testes or penis.

 

Surgical debridements:

100% mortality from Fournier’s gangrene has been reported when surgical debridements not performed (Adinolfi MF, 1983)20, (Okeke LI., 2000)21, (Hasdemir AO, 2009)22.

 

In a study of 43 patients by Ferreira et al., 200718 single debridement was performed in 35 patients, 7 patient’s were debrided twice and 1 patient was debrided thrice. The average number of debridement’s required is 3.5 procedures per patient according to Chawla SN, 200323.

 

In the present series, most patients underwent multiple surgical debridements. Maximum of 7 debridements were done in one patient, single debridement was done in 9 cases, double debridement was done in 11cases, triple debrident was done in 10 patients. The average number of debridements done is 2.7

 

Study

Ferreira et al., 2007

Present study

Max no of debridements

5

7

Single debridement

35 cases

9 cases

Double debridement

7 cases

11 cases

Triple debridement

1 case

10 cases

 

Study

Mean Surgical debridement’s

Chawla S N, 2003

3.5

Present series

2.7

 

RECONSTRUCTIVE PROCEDURES:

After the acute phase of infection has subsided the scrotum can be left alone for healing by secondary intention as it has remarkable capacity to regenerate (Thomas, 1956 24).

 

The reconstructive procedures can be performed at the same time of admission (De la cruz et al., 199625) or after the resolution of acute infectious process. In present study all the reconstructive procedures were performed after resolution of acute infectious process.

 

S Prakash, 1984 26 published a series of 43 cases. In most of the cases cover was provided with scrotal skin for scrotal defects and 58 the penile skin defects were covered with inner layer of prepuce which remained intact.

 

In the present series reconstructive procedure was performed for 17 patients out of 40 (45%). Those 17 patients were managed by primary closure and local skin flap. In that 1 patient required Split skin grafting + Primary closure And 1 patient required Split skin grafting + Implantation of testis in the thigh.

 

Mortality:

Mortality rate from the present study is 15%. The mortality rate from the various series

 

In Baek et al., 2003 clinical study was 6.3%, in Corcoran et al., 2008 clinical study was 10.3%, in Korkut et al., 2003 clinical study was 20%, in Erol et al., 2009 clinical study was 22.2%, in Yeniyol et al., 2004 clinical study was 24%, in Kim KM et al., 2010 Clinical study was 14.8%, in Basoglu et al., 2007 clinical study was 8.9%, in Yilmazler et al., 2010 clinical study was 21.3%, 59 mortality % of present study was similar with Kim KM et al., 2010 study.

 

FGSI SCORE:

The mean FGSI score among survivors in our study is 4.6 +/- 2.0. The mean FGSI score among non-survivors is 10 +/- 1.6. Various other studies have shown FGSI scores as illustrated below.

 

 Study

FGSI – Survival

FGSI – Mortality

Yeniyol et al., 2004

3.0 +/- 1.8

12.0 +/- 2.4

Kim KM et al., 2010

4.7 +/- 0.4

9.3 +/- 3.2

Erol et al., 2010

5.0 +/- 2.9

13.5 +/- 2.6

Laor et al., 1995

6.9 +/- 0.9

13.5 +/- 1.5

Yilmazlar et al.,2010

4

14

Corcoran et al.,2008

5.1 +/- 3.4

10 +/- 4.5

Present series

4.6 +/- 2.0

10 +/- 1.6

 

Laor et al., 1995 have reported that an FGSI score more than 9 indicated 75% probability of mortality whereas a score of 9 or less than 9 was associated with 78% probability of survival.

 

Kabay et al., 2008 proposed that FGSI score of less than 10.5 associated with 96% of survival and FGSI score of more than 10.5 associated with 96% of death. In the present series FGSI score of more than 10.5 is associated with 100% mortality and score of less than 10.5 is associated with 93.3% of survival.

 

SUMMARY AND CONCLUSION SUMMARY

Fourty patients were treated in the katuri medical college and hospital during the period from may 2022 to may 2024. - Highest number of patients was found from fourth and fifth decade of life and the mean age of presentation is 50.2 years. Mean age of presentation among deceased is 63 years which is significantly higher than mean age among survivors which is 48.3 years. - The male to female ratio is 34:6

 

  • The source of the disease is most commonly genitourinary (40%) followed by anorectal (27.5%) and dermatological (12.5%) source. The cause is idiopathic in 20% of cases.
  • Diabetes mellitus (47.5%) is the most common comorbid factor followed by chronic alcoholism (22.5%) and HIV (10%).
  • Most commonly this disease is polymicrobial (80%).
  • Most commonly isolated organisms include E coli (47.0%) followed by streptococci (41.1%) and klebsiella (35.3%).
  • The bacteroides are the most commonly isolated anaerobes (8.9%).
  • In majority of the cases disease is limited to the genitalia (52.9%).
  • Multiple wound debridements are required. The average number of wound debridements required is 2.3.
  • Primary closure was most common reconstructive procedure performed (32.5%).

 

Mortality associated with the disease was 15% - FGSI is a useful indicator for predicting survival and mortality associated with Fournier’s gangrene. - FGSI score of more than 10.5 is associated with 100% mortality and a score lesser than 10.5 is associated with 93.3% of survival

CONCLUSION

Fournier’s gangrene is commonly a disease of middle aged and elderly males. Source of infection is identifiable in most of the cases. Diabetes mellitus is the most common comorbid factor. The disease is polymicrobial in most of the cases. Early diagnosis of the disease and multiple wound debridements are required for improved survival. Extensive raw area following the infection and wound debridements can be managed by reconstructive procedures. In spite of aggressive management the disease carries significant mortality. Fournier’s gangrene severity index (FGSI) is a useful indicator for predicting survival and mortality associated with Fournier’s gangrene.

 

Ethics approval and consent to participate

List of abbrevations

FGSI-fourniers gangrene severity index; Dm-diabetes mellitus

Data Availability

Conflicts of interest

The author’s declare that there is no conflict of interest regarding publication of this paper.

Funding Statement

No Funding

 

Author’s Contributions

Dr. Seelam Srinivasa Reddy (ASSOCIATE PROFESSOR, MS Dept of General Surgery, Katuri Medical College and Hospital, Guntur).

Dr. Prasanth (ASSISTANT PROFESSOR MS Dept of General Surgery, Katuri medical college and Hospital, Guntur).

Dr. Ravipati Sai Krishna (ASSOCIATE PROFESSOR MS Dept of General Surgery, Katuri medical college and Hospital, Guntur).

Acknowledgements

Dr. Pragna Postgraduate in Department of General Surgery, Katuri Medical College and Hospital

Dr. Leela Prasad Postgraduate in Department of General Surgery, Katuri Medical College and Hospital

 

Supplementary Materials

No materials viewed.

REFERENCES
  1. Eke N. (2000) Fournier's gangrene: a review of 1726 cases. Br J Surg. 2000 Jun;87(6):718-28.
  2. Basoglu M, Ozbey I, Atamanalp SS et al. (2007) Management of Fournier’s gangrene: review of 45 cases. Surg Today 37:558–563.
  3. Baek JH, Yoon SJ, Oh JH. (2003) Surgical management of Fournier’s gangrene.J Korean Soc Coloproctol 19:349-53.
  4. Kim KM, Seong SH, Won DY, Ryu H, Kim IY (2010) The Prognostic Factors and Severity Index in Fournier’s Gangrene. J Korean Soc Coloproctol 26:29-33.
  5. Villanueva-Saenz E, Martinez Hernandez-Magro P, Valdes Ovalle M et al (2002) Experience in management of Fournier’s gangrene. Tech Coloproctol 6:5–10.
  6. Yeniyol CO, Suelozgen T, Arslan M, Ayder AR (2004) Fournier’s gangrene: experience with 25 patients and use of Fournier’s gangrene severity index score. Urology 64:218– 222.
  7. Korkut M, Içöz G, Dayangaç M, Akgün E, Yeniay L, Erdoğan O & Cal C. (2003) Outcome analysis in patients with Fournier's gangrene: report of 45 cases Dis Colon Rectum. 2003 May;46(5):649-52.
  8. Eke N. (2000) Fournier's gangrene: a review of 1726 cases. Br J Surg. 2000 Jun;87(6):718-28.
  9. Brunet C, Consentino B, Barthelemy A, Huart L. Gangrenes perineales : new approchesbacteriologiques. Resultats du traitementmedicochirurgical (81 cas). Ann Chir2000;125:420-7.
  10. El Mejjad A, Belmahi A, Choukri A, Kafih M. La gangrènepérinéo-scrotale : à propos de 31 cas. Ann Urol2002;36:277-85.
  11. Corcoran AT, Smaldone MC, Gibbons EP, et al. (2008) Validation of the Fournier’s gangrene severity index in a large contemporary series.J Urol. 180:944-948.
  12. Morpurgo, E. 2002. Galandiuk S. Fournierís gangrene. Surg Clin North Am, 82, 1213-24.
  13. Hong KS, Yi HJ, Lee RA, Kim KH, Chung SS. Prognostic factors and treatment outcomes for patients with Fournier's gangrene: a retrospective study. Int Wound J. 2017 Dec;14(6):1352-1358
  14. Smith GL, Bunker CB & Dinneen MD (1998) Fournier's gangrene. Br J Urol. 1998 Mar;81(3):347-55.
  15. Kuzaka B, Wróblewska MM, Borkowski T, Kawecki D, Kuzaka P, Młynarczyk G, Radziszewski P. Fournier's Gangrene: Clinical Presentation of 13 Cases. Med Sci Monit. 2018 Jan 28;24:548-555.
  16. Proud D., Raiola F., Holden D., Eldho P., Capstick R., Khoo A. (2014) Are we getting necrotizing soft tissue infections right? A 10-year review. ANZ J Surg84: 468–472.
  17. Lewis GD, Majeed M, Olang CA, Patel A, Gorantla VR, Davis N, Gluschitz S. Fournier's Gangrene Diagnosis and Treatment: A Systematic Review. Cureus. 2021 Oct 21.
  18. Ferreira, P. C., Reis, J. C., Amarante, J. M., Silva, A. C., Pinho, C. J., Oliveira, I. C. & Da Silva, P. N. 2007. Fournier's gangrene: a review of 43 reconstructive cases. Plastic and reconstructive surgery, 119, 175.
  19. Thwaini, A., Khan, A., Malik, A., Cherian, J., Barua, J., Shergill, I. & Mammen, K. 2006. Fournierís gangrene and its emergency management. Postgraduate medical journal, 82, 516.
  20. Adinolfi MF, Voros DC, Moustouskas NM, Hardin WD, Nichols RL. Severe systemic sepsis resulting from neglected perineal infections. South Med J 1983; 76: 746-749.
  21. Okeke LI. Fournier's gangrene in Ibadan. Afr J Med Med Sci 2000; 29:323–324.
  22. Hasdemir AO, Buyukasik O, Col C. The clinical characteristics of female patients with Fournier's gangrene. Int Urogynecol J Pelvic Floor Dysfunct. 2009; 20:1439-1443.
  23. Chawla SN, Gallop C, Mydlo JH. Fournier’s gangrene: An analysis of repeated surgical debridement. EurUrol 2003;43: 572-5.
  24. Thomas, J. 1956. Fournier's gangrene of the penis and the scrotum. The Journal of urology, 75, 719.
  25. Karian LS, Chung SY, Lee ES. Reconstruction of Defects After Fournier Gangrene: A Systematic Review. Eplasty. 2015 May 26;15
  26. Parkash and V. Gajendran, “Surgical reconstruction of the sequelae of penile and scrotal gangrene: a plea for simplicity,” British Journal of Plastic Surgery, vol. 37, no. 3, pp. 354–3

 

Recommended Articles
Research Article
Assessement of Deitary Habits, Nutritional Status and Dietary Knowledge of Medical Students of SMS Medical College Jaipur.
...
Published: 12/03/2025
Download PDF
Research Article
A Comparative Study of Merits and Demerits of Exteriorization of Uterus During Cesarean Delivery
...
Published: 17/03/2025
Download PDF
Research Article
A Clinico-Pathological Correlation Study of Fibroid Uterus in KIMS Hospital
...
Published: 17/03/2025
Download PDF
Research Article
Knowledge, Attitude, and Practices of Contraception Among Married Women Attending Family Planning Clinics at a Tertiary Care Centre
...
Published: 17/03/2025
Download PDF
Chat on WhatsApp
Copyright © EJCM Publisher. All Rights Reserved.