CC BY-NC-ND 4.0 · Indian J Plast Surg
DOI: 10.1055/s-0044-1785489
Original Article

Post-COVID-19 Rhino-Orbito-Maxillary Mucormycosis Defect: Our Surgical Experience with Single Stage Delayed Reconstruction Using Free Flap

1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
Prakash Chandra Kala
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
Priyanka Singla
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
,
Apoorva Pratap Singh
1   Department of Burns and Plastic Surgery, All India Institute of Medical Science, Jodhpur, Rajasthan, India
› Author Affiliations
 

Abstract

Introduction The effect of the second wave of COVID-19 was immense in India, specifically in the form of vicious COVID-19-associated mucormycosis. A higher number of radical debridements are required for disease control in combination with antifungal drugs in cases of COVID-19-associated mucormycosis, which results in complex maxillofacial defects. We aimed to evaluate the clinical outcomes in patients with rhino-orbito-maxillary defects due to COVID-19-associated mucormycosis undergoing a single stage delayed free flap reconstruction.

Methodology This prospective, single-center, multisurgeon study was performed on eight patients with COVID-19-associated rhino-orbito-maxillary mucormycosis in the department of burns and plastic surgery. The postoperative clinical outcome was evaluated using the University of Washington Quality of Life Questionnaire for patient's quality of life (QOL), aesthetic numeric analog (ANA) scale for patient's satisfaction for aesthetics, and the functional intraoral Glasgow scale for speech and deglutition at 1 and 3 months.

Results The median age of the study patients was 40 years, with 75% of the patients being males. Diabetes mellitus (DM) was present in all the patients. Mucormycosis was diagnosed within the first 3 months of COVID-19 infection. Maxillary defect was present in 62.5% of patients, out of which 50% had bilateral maxillary defects. There was significant improvement in the QOL and the aesthetics of patients from 1 to 3 months (p < 0.001). Speech and deglutition were also improved at 3 months, but the difference was not statistically significant.

Conclusion Single stage delayed free flap reconstruction can be advocated in patients with COVID-19-associated rhino-orbito-maxillary mucormycosis defect as there is considerable improvement in patients' QOL, aesthetics, speech, and deglutition over a period of time.


#

Introduction

The effect of the second wave of COVID-19 was immense in India, specifically in the form of the vicious COVID-19-associated mucormycosis,[1] which was commonly referred to as the “black fungus.”[2] Of the total number of mucormycosis cases reported till June 2021, 86% of the cases had a history of COVID-19 infection, and a history of diabetes mellitus (DM) was present in 62% of patients.[3] Generally, a higher number of radical debridement are required for disease control in combination with antifungal drugs in cases of COVID-19-associated mucormycosis. Most of these patients require adjuvant surgeries including orbital exenteration, sinus and thoracic cavity debridement, lung resection, and decortication, which leads to complex tissue defects involving the maxillofacial region. Thus, it is anticipated that most of the survivors of COVID-19-associated mucormycosis will approach for reconstruction surgeries over a period of time.[1] Numerous cases series have described the clinical presentation, radiological investigations, neurological aspect, and management of patients with COVID-19-associated mucormycosis,[4] [5] [6] [7] [8] [9] and various local flaps like submental flap, facial artery musculomucosal flap, and various free flap including radial artery forearm free flap, deep circumflex iliac artery flap, anterolateral thigh (ALT) flap, and free fibula flap, but none of the studies have included details regarding the postoperative clinical outcomes of delayed reconstructive surgeries performed for rhino-orbito-maxillary (ROM) defects that occurred due to COVID-19-associated mucormycosis with DM. This study was conducted to evaluate the clinical outcomes in view of the quality of life, aesthetics, speech, and deglutition for short duration in patients with ROM defects due to COVID-19-associated mucormycosis with DM undergoing single stage delayed free flap reconstruction.


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Methodology

This prospective, single-center, multisurgeon study was performed on eight patients with COVID-19-associated ROM mucormycosis defect undergoing delayed single stage free flap reconstruction in the burns and plastic surgery department and fulfilling the inclusion and exclusion criteria. Patients with confirmed diagnosis of COVID-19-associated postmucormycosis ROM defect, who had complete resolution of the disease process, were eligible for free flap reconstruction, and were willing to give written informed consent were included in the study, while patients with an active form of disease and defect due to causes other than COVID-19-associated mucormycosis were excluded from the study.

In all patients, proper history, examination (wound assessment), radiological workup, and preanesthetic checkup (with routine investigations) were done and recorded in a predesigned proforma ([Figs. 1] and [2]). Written informed consent for the procedure was obtained from each patient prior to their enrollment in this study, so as to ensure patients' willingness to participate in the study. All the patients were briefed about the study and were given “patient information sheet.” The surgical procedure was performed under general anesthesia after debridement ([Figs. 3] and [4]). Regular follow-up of the patient was done. Patient's satisfaction with the appearance of the reconstructed area was evaluated using the aesthetic numeric analog scale (ANA), quality of life was evaluated using the University of Washington Quality of Life Questionnaire (UW-QOL),[10] and speech and deglutition were evaluated by using the functional intraoral Glasgow scale (FIGS). All these parameters were evaluated postoperatively at 1 and 3 months. The questionnaire was presented to the participants by a resident of the plastic surgery department who was not part of the study and the parameters were evaluated at 1 and 3 months by the same resident. The study was conducted in accordance with the ethical guidelines of Declaration of Helsinki, which are consistent with the good clinical practice (GCP) and applicable regulatory requirements. Data thus collected were entered in a Microsoft Excel Sheet and were subjected to statistical analysis. Statistical analysis was performed with help of Epi Info 7.2.2.2. Epi Info is a trademark of the Centers for Disease Control and Prevention (CDC). Descriptive statistical analysis was performed to calculate the means with corresponding standard deviations (s.d.). Test of proportion was used to find the standard normal deviate (Z) to compare the difference in proportions. The t-test was used to compare two means. A p value less than 0.05 was considered statistically significant.

Zoom Image
Fig. 1 Preoperative clinical picture of a patient with a orbitomaxillary defect: (A) frontal view, (B) right oblique view, and (C) orbital defect. Computed tomography (CT) scan three-dimensional (3D) reconstruction view: (D) anterior and (E) right oblique views.
Zoom Image
Fig. 2 Preoperative clinical picture of a patient with a rhinomaxillary defect: (A) frontal view, (B) right lateral view, and (C) palatal defect. Computed tomography (CT) scan three-dimensional (3D) reconstruction view: (D) anterior view and (E) left lateral views.
Zoom Image
Fig. 3 Intraoperative picture of a patient with an orbitomaxillary defect: (A) flap marking; (B) orbitomaxillary defect; and (C) immediate postoperative picture. Postoperative follow-up pictures of the patient at 3 months: (D) frontal, (E) right oblique, and (F) right lateral views.
Zoom Image
Fig. 4 Intraoperative picture of a patient with rhinomaxillary defect: (A) flap marking; (B) flap harvesting; and (C) rhinomaxillary defect. Postoperative follow-up pictures at 3 months: (D) frontal, (E) right lateral, and (F) intraoral views.

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Results

The mean age of the study patients was 42.38 ± 12.42 years, with a range of 25 to 63 years. In all, 62.5% of the patients were below 50 years of age. The majority of patients were males (75%), with a male-to-female ratio of 3:1. DM was present as a comorbidity in all the patients. Smoking habit was observed in 37.5% of patients. Six of eight patients was diagnosed with mucormycosis within the first 3 months of COVID-19 infection. A maxillary defect was present in 62.5% of patients, out of which 50% had bilateral maxillary defects (p < 0.0001). An orbital defect was present in 37.5% of patients. Delayed surgery was performed within 12 months in seven patients and after 24 months in one patient ([Table 1]).

Table 1

Demographic details of study patients

Patient no.

Age (y)

Gender

Comorbidity

Habits

Mucor after COVID-19 infection (d)

Defect after operation

Delayed surgery (d)

No. of debridements before reconstruction

1

33

M

DM

Nil

90

Bilateral maxilla defect

270

03

2

35

M

DM

Tobacco chewing

60

Bilateral maxilla defect

180

02

3

51

M

DM

Smoking

160

Right orbital defect

210

02

4

44

M

DM

Smoking and opium addiction

90

Bilateral total maxilla defect

90

02

5

25

M

DM

None

60

Bilateral total maxilla defect

120

03

6

36

M

DM

Smoking

90

Right orbital defect

270

03

7

52

F

DM

None

150

Right maxilla defect

330

04

8

63

F

DM

Tobacco chewing

90

Left orbital defect

720

04

In 87.5% of patients, the size of the flap was more than 50 cm2. Out of the three different types of free flaps performed in this study, free fibula flap (62.5%) was significantly higher than free ALT flaps (25%) and free vastus lateralis (VL) muscular flaps (12.5%), with Z = 1.99 and p = 0.044. In 75% of cases, the duration of surgery was ≤6 hours, which was significant (Z = 7.07; p < 0.0001). Facial artery was the recipient artery in seven of eight cases. In all eight patients, one artery and one vein anastomoses were performed. Donor area management was done by skin grafting (62.5%) and primary closure (37.5%). Complete flap loss was observed in two patients; extraoral medial wound dehiscence, hematoma, and intraoral wound dehiscence were observed in one patient each; and no complications were observed in three patients. Secondary procedures were performed in three patients and donor site complication was observed in only one out of eight patients. The duration of hospital stay was up to 3 weeks in 62.5% of patients ([Table 2]).

Table 2

Surgical details of study patients

Flap size

Free flap

Type of flap

Recipient artery

Artery and vein anastomosis

Duration of surgery (min)

Donor area management

Complications flap

secondary procedure

Donor site complication

Secondary procedure for donor site

Hospitalization days

60 cm2

Free fibula flap

Osteocutaneous flap

Facial artery

1 artery and 1 vein

300

Skin grafting

Hematoma wound

Nasolabial

None

None

21

48 cm2

Free fibula flap

Osteocutaneous flap

Facial artery

1 artery and 1 vein

330

Skin grafting

None

None

None

None

23

72 cm2

Free ALT

Fasciocutaneous flap

Superficial temporal artery

1 artery and 1 vein

300

Primary closure

Complete loss

None

None

None

20

66 cm2

Free fibula flap

Osteocutaneous flap

Facial artery

1 artery and 1 vein

330

Skin grafting

None

None

None

None

10

56 cm2

Free fibula flap

Osteocutaneous flap

Facial artery

1 artery and 1 vein

360

Skin grafting

Complete loss

None

No

None

7

78 cm2

Free ALT

Fasciocutaneous flap

Facial artery

1 artery and 1 vein

480

Primary closure

Intraoral wound dehiscence

Radial artery forearm flap

None

None

23

60 cm2

Free fibula flap

Osteocutaneous flap

Facial artery

1 artery and 1 vein

360

Skin grafting

Extraoral medial wound dehiscence

Resetting of flap

Marginal loss STSG

Secondary healing

40

84 cm2

Free VL muscular flap

Muscle flap

Facial artery

1 artery and 1 vein

480

Primary closure

None

None

None

None

25

Abbreviations: ALT, anterolateral thigh flap; STSG, split-thickness skin graft; VL, vastus lateralis.


At 1 month, only 16.7% of study patients reported very good QOL, while 66.7% patients reported very good QOL at 3 months, suggestive of significant improvement from 1 to 3 months ([Table 3]). Similarly, the mean ANA score also improved significantly from 1 month (7.33 ± 0.82) to 3 months (8.67 ± 1.21). Speech and deglutition also showed improvement in all the patients from 1 to 3 months, but it was not statistically significant (p > 0.001; [Table 4]). Improvement in the speech of the patient with an orbitomaxillary defect and rhinomaxillary defect can be observed in [Videos 1] and [2], respectively.

Table 3

Quality of life (QOL) at 1 and 3 months

QOL

At 1 mo

At 3 mo

Number

%

Number

%

Very good

1

16.7

4

66.7

Good

5

83.3

2

33.3

Total

6

100.0

6

100.0

Table 4

Postoperative parameters at 1 and 3 months

Parameters

Mean

Median

Range

ANA

At 1 mo

7.33 ± 0.82

7.5

6–8

At 3 mo

8.67 ± 1.21

8.5

7–10

Speech

At 1 mo

3.33 ± 0.52

3

3–4

At 3 mo

3.83 ± 0.41

4

3–4

Deglutition

At 1 mo

4.17 ± 0.75

4

3–5

At 3 mo

4.67 ± 0.52

5

4–5

Abbreviation: ANA, aesthetic numerical analog.


Video 1 Postoperative outcome using Free ALT flap at three months.


Quality:

Video 2 Postopertaive outcome using Free fibula flap at three months.


Quality:

#

Discussion

Epidemiological studies have indicated that rhino-orbito-cerebral mucormycosis (ROCM) is the most commonly encountered variant of COVID-19-associated mucormycosis.[11] India has experienced a relatively higher number of COVID-19-associated mucormycosis cases. Clinical presentation of COVID-19-associated mucormycosis was similar to the ROCM commonly seen in diabetic patients.[12] Recent reports support a strong association between COVID-19, corticosteroid therapy, and mucormycosis, although preexisting immunosuppressive conditions like DM should be considered as strong confounders.[13] Radical debridement is the most important surgical step that involves thorough debridement of all sites without leaving behind any residual disease. However, large-volume excision results in huge anatomical defects, and reconstruction in such cases is often grueling. We conducted this study to investigate the short-term clinical outcomes of single stage delayed free flap reconstruction surgery in patients with ROM defects due to COVID-19-associated mucormycosis in terms of the quality of life, aesthetics, speech, and deglutition.

In our study, 5 of 8 patients were below 50 years of age. Agrawal et al[4] observed that most of the patients with COVID-19-associated ROM mucormycosis were in the age group of 40 to 50 years. However, in most of the cases of COVID-19-associated mucormycosis reported in the literature, patients were older 50 years.[5] [8] [14] [15] This may be because our study included survivors of COVID-19-associated mucormycosis, who came for reconstructive surgeries after complete resolution of the disease. Mortality rate is higher in COVID-19-associated mucormycosis and chances of survival are higher in younger patients with better immunity and lesser comorbidities.

In our study, male dominance was observed in patients with COVID-19-associated ROM mucormycosis defects. Another study involving patients with COVID-19-associated ROM mucormycosis reported that 66.67% of patients were males.[4] In a recent review on cases with COVID-19-associated mucormycosis from 18 countries, Hoenigl et al[14] observed that 78% of the patients affected by this disease were males. This is in accordance with the previous studies that suggested male dominance among patients with COVID-19-associated mucormycosis.[6] [8] [9] [14]

ROCM represents the commonest clinical form of mucormycosis in the Indian population and around 88% of these cases are associated with DM.[7] [16] All the patients in our study were diabetic. Similarly, all the four patients with COVID-19-associated mucormycosis were diabetic in a recent case series by Roushdy and Hamid.[8] Balushi et al[6] also observed uncontrolled blood glucose levels in all 10 patients with COVID-19-associated mucormycosis in their case series. DM was also present in the majority of the patients with COVID-19-associated mucormycosis reported in the literature.[4] [5] [14] [15]

In our study, 2 of 8 patients were diagnosed with COVID-19-associated mucormycosis within 2 months of COVID-19 infection, 4 patients were diagnosed in the third month, 1 patient after 5 months, and 1 patient after 160 days of COVID-19 infection. Various surgical procedures that were performed in each of these patient as a part of the management protocol included bilateral (B/L) maxillectomy along with an alveolar process and hard palate removal (patient 1); B/L infrastructure maxillectomy + B/L frontal sinusotomy (patient 2); right maxillectomy with orbital exenteration (patient 3); B/L maxillectomy involving anterior two-thirds hard palate with B/L frontal and ethmoidal sinusotomy (patient 4); B/L maxillectomy with B/L ethmoidal and maxillary sinusotomy (patient 5); right maxillectomy including alveolar process along with a bony defect wall of the maxillary and frontal sinus with right orbital exenteration (patient 6); right maxillectomy along with removal of the right zygoma, maxillary sinus, and right pterygoid plate (patient 7); and left suprastructure maxillectomy along with orbital exenteration (patient 8). This resulted in complex maxillofacial defects in patients postoperatively. Four patients presented with a B/L maxillary defect, three patients presented with an orbital defect, and one patient with a unilateral maxillary defect. Seven of eight patients presented within 12 months duration in whom surgery was performed within 1 year, while one patient presented after 24 months.

The mean flap size used in our study was 64.75 ± 11.21 cm2, with a range of 48 to 84 cm2. In most of the patients, the flap size was between 51 and 75 cm2. Out of eight patients, osteocutaneous free fibula (OFF) flap was performed in five patients, fasciocutaneous free ALT (FF-ALT) flap was done in two patients, and free VL muscular (FVLM) flap was performed in one patient. The recipient artery was the superficial temporal artery in one patient who underwent reconstruction using FF-ALT flaps, whereas in the rest of the patients, the facial artery was used accompanied with anastomosis between an artery and a vein. Duration of surgery ranged from 5 to 8 hours, with a median of 5 hours and 45 minutes. Primary closure at the donor site was done in patients who underwent FF-ALT flap (n = 2) and FVLM flap reconstruction (n = 1), while skin grafting was done in all patients who underwent OFF flap reconstruction (n = 5).

The majority of the cases of post- COVID-19-associated ROM defect reported in the literature have been rehabilitated prosthetically using intraoral obturators, partial dentures, palatal flaps, and other soft-tissue flaps.[5] [17] A recent study by Gupta et al[18] used ALT flaps for covering COVID-19-associated mucormycosis defects in 14 patients. All flaps in their study survived, without any major or minor complications. However, in our study, complete flap loss was observed in two cases, wound dehiscence was observed in two cases, and hematoma was observed in one case. In our study, no complications were reported in three of eight patients, out of which two underwent a reconstruction using an OFF flap and one an FVLM flap reconstruction. Complete flap loss was observed in one patient who underwent an FF-ALT flap reconstruction and in a patient who underwent an OFF flap reconstruction. Hematoma was observed in one patient who received an OFF flap, intraoral wound dehiscence was observed in one patient who underwent an FF-ALT flap reconstruction and extraoral medial wound dehiscence was observed in one patient with an OFF flap reconstruction. In one patient, reconstructive surgery was performed using an ALT free flap to cover the complex orofacial defect after cessation of the disease process; unfortunately, the patient died in intensive care unit (ICU) postoperatively.[9]

Secondary procedures were performed in patients with complications in flaps except for those with complete loss of flap. Marginal loss of split-thickness skin graft (STSG) was observed at the donor site in a patient who suffered extraoral medial wound dehiscence, which healed by secondary healing. The length of hospital stay was 1 week for 1 patient, 2 weeks for 1 patient, 3 weeks for 2 patients, 4 weeks for 3 patients, and more than 4 weeks for 1 patient.

We evaluated the postoperative clinical outcomes using the UW-QOL[10] for the quality of life of patients, ANA scale for patient satisfaction for aesthetics, and FIGS for speech and deglutition at 3 and 6 months. There was significant improvement in the QOL and aesthetics of patients from 1 to 3 months (p < 0.001). Speech and deglutition were also improved at 3 months, but the difference was not statistically significant (p > 0.001). To the best of our knowledge, ours is the first study that has evaluated the postoperative outcome of single stage delayed free flap reconstructive surgery in patients with ROM defects due to COVID-19-associated mucormycosis in terms of QOL, ANA, speech, and deglutition.


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Conclusion

COVID-19-associated ROM mucormycosis is a serious life-threating complication of COVID-19, which has a very low survival rate. Survivors of this disease frequently present with complex maxillofacial defects after few months that need reconstructive surgeries for acceptable aesthetics. Single stage delayed free flap reconstructive surgery can be a reliable procedure in such patients as it improves patients' QOL, aesthetics, speech, and deglutition over time.


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Conflict of Interest

None declared.

  • References

  • 1 Cheruvu VPR, Khan MM. Reconstruction in rhino-orbito-cerebral mucormycosis survivors: a systematic review. Eplasty 2022; 22: e20
  • 2 Singh P. Black fungus: here is a list of states with highest number of mucormycosis cases. Hindustan Times. Published May 21, 2021. Accessed June 17, 2021 at: https://www.hindustantimes.com/india-news/black-fungus-states-with-highest-number-of-mucormycosis-cases-101621559394002.html
  • 3 Zee Media Bureau. 28,252 mucormycosis cases with 86% history of COVID from 28 states/UTs: Harsh Vardhan. Zee News. Published June 7, 2021. Accessed June 17, 2021 at: https://zeenews.india.com/india/28252-mucormycosis-cases-with-86-history-of-covid-from-28-states/uts-harsh-vardhan-2367455.html
  • 4 Agrawal A, Dixit Y, Yonati V, Nigam P, Kheti P. Imaging of COVID-19-associated rhino-orbital-cerebral mucormycosis: imaging analysis of 120 patients. Egypt J Otolaryngol 2022; 38: 154
  • 5 Sneha A, Kumar M P S, Krishnan M, Dhasarathan P. O R Muralidoss H. Resection and rehabilitation for COVID-19 associated rhino-maxillary mucormycosis: a case report. Cureus 2023; 15 (05) e39670
  • 6 Balushi AA, Ajmi AA, Sinani QA. et al. COVID-19-associated mucormycosis: an opportunistic fungal infection. A case series and review. Int J Infect Dis 2022; 121: 203-210
  • 7 Ravi MB, Srinivas S, Silina E, Sengupta S, Tekwani T, Achar RR. Prosthetic rehabilitation of rhino orbital mucormycosis associated with COVID-19: a case series. Clin Cosmet Investig Dent 2022; 14: 1-10
  • 8 Roushdy T, Hamid E. A case series of post COVID-19 mucormycosis-a neurological prospective. Egypt J Neurol Psychiat Neurosurg 2021; 57 (01) 100
  • 9 Saad RH, Mobarak FA. The diversity and outcome of post-covid mucormycosis: a case report. Int J Surg Case Rep 2021; 88: 106522
  • 10 Rogers SN, Gwanne S, Lowe D, Humphris G, Yueh B, Weymuller Jr EA. The addition of mood and anxiety domains to the University of Washington quality of life scale. Head Neck 2002; 24 (06) 521-529
  • 11 Bumbasirevic M, Stevanovic M, Bumbasirevic V. There are free fibular grafts. Int Orthop 2014; 38: 1277-1282
  • 12 John TM, Jacob CN, Kontoyiannis DP. When uncontrolled diabetes mellitus and Severe COVID-19 converge: the perfect storm for mucormycosis. J Fungi (Basel) 2021; 7 (04) 298
  • 13 Vekris BA. and others. Lower limb reconstruction involves the transfer of bones. Microsurgery 2011; 31 (03) 205-211
  • 14 Hoenigl M, Seidel D, Carvalho A. et al; ECMM and ISHAM collaborators. The emergence of COVID-19 associated mucormycosis: a review of cases from 18 countries. Lancet Microbe 2022; 3 (07) e543-e552
  • 15 Sethi HS, Sen KK, Mohanty SS, Panda S, Krishna KR, Mali C. COVID-19-associated rhino-orbital mucormycosis (CAROM)—a case report. Egypt J Radiol Nucl Med 2021; 52: 165
  • 16 Prakash H, Ghosh AK, Rudramurthy SM. et al. A prospective multicenter study on mucormycosis in India: epidemiology, diagnosis, and treatment. Med Mycol 2019; 57 (04) 395-402
  • 17 Artopoulou II, Kalfarentzos E, Polyzois G, Perisanidis C. Prosthodontic restoration of a COVID-19 associated mucormycosis defect: a clinical report. Spec Care Dentist 2023; 43 (05) 696-700
  • 18 Gupta S, Goil P, Mohammad A, Escandón JM. Mucormycosis management in COVID-19 era: is immediate surgical debridement and reconstruction the answer?. Arch Plast Surg 2022; 49 (03) 397-404

Address for correspondence

Akhilesh Humnekar, MS, MCh (Plastic Surgery)
Department of Burns and Plastic Surgery, All India Institute of Medical Science
Jodhpur, Rajasthan
India   

Publication History

Article published online:
23 April 2024

© 2024. Association of Plastic Surgeons of India. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Cheruvu VPR, Khan MM. Reconstruction in rhino-orbito-cerebral mucormycosis survivors: a systematic review. Eplasty 2022; 22: e20
  • 2 Singh P. Black fungus: here is a list of states with highest number of mucormycosis cases. Hindustan Times. Published May 21, 2021. Accessed June 17, 2021 at: https://www.hindustantimes.com/india-news/black-fungus-states-with-highest-number-of-mucormycosis-cases-101621559394002.html
  • 3 Zee Media Bureau. 28,252 mucormycosis cases with 86% history of COVID from 28 states/UTs: Harsh Vardhan. Zee News. Published June 7, 2021. Accessed June 17, 2021 at: https://zeenews.india.com/india/28252-mucormycosis-cases-with-86-history-of-covid-from-28-states/uts-harsh-vardhan-2367455.html
  • 4 Agrawal A, Dixit Y, Yonati V, Nigam P, Kheti P. Imaging of COVID-19-associated rhino-orbital-cerebral mucormycosis: imaging analysis of 120 patients. Egypt J Otolaryngol 2022; 38: 154
  • 5 Sneha A, Kumar M P S, Krishnan M, Dhasarathan P. O R Muralidoss H. Resection and rehabilitation for COVID-19 associated rhino-maxillary mucormycosis: a case report. Cureus 2023; 15 (05) e39670
  • 6 Balushi AA, Ajmi AA, Sinani QA. et al. COVID-19-associated mucormycosis: an opportunistic fungal infection. A case series and review. Int J Infect Dis 2022; 121: 203-210
  • 7 Ravi MB, Srinivas S, Silina E, Sengupta S, Tekwani T, Achar RR. Prosthetic rehabilitation of rhino orbital mucormycosis associated with COVID-19: a case series. Clin Cosmet Investig Dent 2022; 14: 1-10
  • 8 Roushdy T, Hamid E. A case series of post COVID-19 mucormycosis-a neurological prospective. Egypt J Neurol Psychiat Neurosurg 2021; 57 (01) 100
  • 9 Saad RH, Mobarak FA. The diversity and outcome of post-covid mucormycosis: a case report. Int J Surg Case Rep 2021; 88: 106522
  • 10 Rogers SN, Gwanne S, Lowe D, Humphris G, Yueh B, Weymuller Jr EA. The addition of mood and anxiety domains to the University of Washington quality of life scale. Head Neck 2002; 24 (06) 521-529
  • 11 Bumbasirevic M, Stevanovic M, Bumbasirevic V. There are free fibular grafts. Int Orthop 2014; 38: 1277-1282
  • 12 John TM, Jacob CN, Kontoyiannis DP. When uncontrolled diabetes mellitus and Severe COVID-19 converge: the perfect storm for mucormycosis. J Fungi (Basel) 2021; 7 (04) 298
  • 13 Vekris BA. and others. Lower limb reconstruction involves the transfer of bones. Microsurgery 2011; 31 (03) 205-211
  • 14 Hoenigl M, Seidel D, Carvalho A. et al; ECMM and ISHAM collaborators. The emergence of COVID-19 associated mucormycosis: a review of cases from 18 countries. Lancet Microbe 2022; 3 (07) e543-e552
  • 15 Sethi HS, Sen KK, Mohanty SS, Panda S, Krishna KR, Mali C. COVID-19-associated rhino-orbital mucormycosis (CAROM)—a case report. Egypt J Radiol Nucl Med 2021; 52: 165
  • 16 Prakash H, Ghosh AK, Rudramurthy SM. et al. A prospective multicenter study on mucormycosis in India: epidemiology, diagnosis, and treatment. Med Mycol 2019; 57 (04) 395-402
  • 17 Artopoulou II, Kalfarentzos E, Polyzois G, Perisanidis C. Prosthodontic restoration of a COVID-19 associated mucormycosis defect: a clinical report. Spec Care Dentist 2023; 43 (05) 696-700
  • 18 Gupta S, Goil P, Mohammad A, Escandón JM. Mucormycosis management in COVID-19 era: is immediate surgical debridement and reconstruction the answer?. Arch Plast Surg 2022; 49 (03) 397-404

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Fig. 1 Preoperative clinical picture of a patient with a orbitomaxillary defect: (A) frontal view, (B) right oblique view, and (C) orbital defect. Computed tomography (CT) scan three-dimensional (3D) reconstruction view: (D) anterior and (E) right oblique views.
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Fig. 2 Preoperative clinical picture of a patient with a rhinomaxillary defect: (A) frontal view, (B) right lateral view, and (C) palatal defect. Computed tomography (CT) scan three-dimensional (3D) reconstruction view: (D) anterior view and (E) left lateral views.
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Fig. 3 Intraoperative picture of a patient with an orbitomaxillary defect: (A) flap marking; (B) orbitomaxillary defect; and (C) immediate postoperative picture. Postoperative follow-up pictures of the patient at 3 months: (D) frontal, (E) right oblique, and (F) right lateral views.
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Fig. 4 Intraoperative picture of a patient with rhinomaxillary defect: (A) flap marking; (B) flap harvesting; and (C) rhinomaxillary defect. Postoperative follow-up pictures at 3 months: (D) frontal, (E) right lateral, and (F) intraoral views.