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IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 14, Issue 11 Ver. II (Nov. 2015), PP 38-40
www.iosrjournals.org
DOI: 10.9790/0853-141123840 www.iosrjournals.org 38 | Page
Giant Vulvar Elephantiasis of Filarial Origin: A Rare Case
Report
Satish Kumar Ranjan4*
, Mini Sinha3
, Nawal K Jha1
, D K Sinha2
,
Amrisha Sharan4
1. Prof & Head , Department of general surgery , RIMS , Ranchi, India
2. Associate professor , department of general surgery ,RIMS , Ranchi, India
3. Senior resident , department of general surgery , RIMS , Ranchi, India
4. Junior resident , department of general surgery , RIMS , Ranchi ,India
*Corresponding author: Dr Satish Kumar Ranjan
Hostel no. 5 , room no. 43 RIMS , Bariatu , Ranchi-834009
Email id : docsatis48@gmail.com
Abstract: Genital lymphedema is rare outside the endemic filariasis regions. Elephantiasis is the manifestation
of chronic lymphedema. Involvement of limbs, trunk and male genitelia is common but elephantiasis of vulvar
origin is rare even in endemic areas. we report a case of giant vulval elephantiasis in a young female. A 21 year
old unmarried female presented with swelling of bilateral labia since 7 years with dragging pain and
discomfort . Patient was managed by excision of filarial tumor with vulvoplasty and discharged uneventfully.
Keywords: Elephantiasis , Lymphedema, Vulval , , Wuchereria bancrofti
I. Introduction
Genital elephantiasis is caused by a variety of infective and non infective causes leading to blockage of
lymphatics. Vulvar elephentiasis is rare and it accounts of only 1-2% of total elephantiasis (1) . Greek
terminology Esthioneme used to describe elephantiasis which means to eat and carries an idea something
gnawed, eroded or ulcerated (2). Etiology of elephantiasis may be filarial , tubercular , chlamydial infection ,
post vulvectomy , post radiotherapy, after inguinal and pelvic lymph node dissection or idiopathic (3,4).
Commonest infective Filariasis results from infection with Wuchereria bancrofti and Brugia malayi. Wuchereria
bancrofti accounts for 90% of the case of human lymphatic filariasis. Nonlymphatic filarisis is caused by
onchocera volvulus, loa loa or mansonella perstans. Lymphedema is due to accumulation of protein rich
interstitial fluids, leads to proliferation of fibroblasts and mast cell , edema fluid organised progressively and
fibrosis of the subcutaneous tissue giving rise to irreversible , firm and non pitting swelling. Hyperkeratosis,
ruggosities , verrucous and condylomatous changes are features of long-standing lymph stasis and are
collectively termed ‘elephantiasis”(5)
II. Case Report
A 21 year old unmarried girl presented in department of general surgery of Rajendra institute of
medical sciences , Ranchi ,India with mild grade fever , dragging pain and swelling in genital area with
difficulty in walking and working normally since 7years. Patient was also in significant psychological distress.
There was no history of trauma , previous surgeries , radiotherapy, or chyluria .No history of swelling
since childhood or lymphedema in family. All general and systemic examinations were within normal limit.
On laboratories examinations Hb-10.5gm/dl , leukocyte count 10,400 cells/mm3, neutrophilia of 72%,
lymphocyte 17% , eosinophil 08% , ESR 50mm in first hour was found. Patient was hepatitis B positive
(HBsAg) with titer <6 IU/ml.
On local examination bilateral vulval swelling was found [ fig. 1] . Size of swellings were 21x14 cm on
left side and 7x4 cm on right side with illdefined margin , irregular bosselated surface, firm in consistency ,
freely mobile. There was no ulceration or lymphadenopathy.
Cinical diagnosis of vulvar filariasis was made and total excision of tumor mass done under spinal
anesthesia [fig. 2]. Two large irregular mass of weighs about 6 kg and 2 kg was excised [fig. 3].
Histopathological reports showed proliferation of stratified squamous epithelium showing acanthosis
and increased junctional activity with Interlacing band of fibroblasts and collagen and perivascular mixed
inflammatory infiltrate[fig. 4] . ZN and PAS staining was negative. Filarial antigen assay was positive. Pelvic
ultrasonography was unremarkable.
Giant vulvar elephantiasis of filarial origin: a rare case report
DOI: 10.9790/0853-141123840 www.iosrjournals.org 39 | Page
III. Discussion
The term elephantiasis was first described by Celsius (30BC-50AD) (6). Lymphatic filariasis of
external genitelia was first described in 1673. Vulval lymphedema can be a rare extraintestinal manifestation of
Crohn’s disease (7,8). Differential diagnosis includes genital warts, lymphogranuloma, Lymphangioma
circumscriptum, and fibro epithelial polyp, fungal infection, and carcinoma and angiomyxoma (9,10).
Diagnosis of elephantiasis is mainly clinical and supported by histopathological examination. Neither
microfilarae in blood nor adult worm in tissue can Found all the times (not sensitive).
Treatment of filarial lymphedema is Diethylcarbamazine (DEC) in three divided doses of 6 mg/kg/day
for 21 days kills adults and microfilarae. Leg elevation , elastic stocking , decongestive physiotherapy and
maintenance of good skin care is also recommended. Surgical treatments includes excision of skin and
subcutaneous tissue of involved part and primary closure of defect with normal adjacent skin. Partial thickness
graft or rotation flap can be used if raw area is large.
Surgical treatment is used only in extreme cases in order to reduce the weight of the affected organ, to
help minimize the frequency of inflammatory attacks, to improve cosmesis, and to potentially reduce the risk of
secondary angiosarcoma.(11,12).
In our case patient came with large vulval swelling with difficulty in walk and work normally, after
excision of mass we improved her life style and also provide good cosmosis which decreases her anxiety about
future marital status. Rare presentation of our case evoks us to report the case.
IV. Figure
Figure 1 . Bilateral vulvar elephantiasis
Figure 2. –Surgical excision of filarial tumor
Giant vulvar elephantiasis of filarial origin: a rare case report
DOI: 10.9790/0853-141123840 www.iosrjournals.org 40 | Page
Figure 3- Specimen obtained after excision
Figure 4. – Histopathological report showing acanthosis and increased junctional activity with
Interlacing band of fibroblasts and collagen and perivascular mixed inflammatory infiltrate.
V. Conclusion
Although genital elephantiasis is rare in developed countries, it is still a challenge for tropics and
subtropics. Genital elephantiasis significantly affect physical, social as well as mental status of the patient. So
early detection and treatment of lymphedema is only option to prevent it.
References
[1]. Khanna NN, Joshi GK. Elephantiasis of female genitalia. Case peport. Plast Reconstr Surg 1971;48(4):379-81.
[2]. Sharma K, Gupta S, Naithani U, Gupta S. Huge vulval elephantiasis Anesthetic management for caesarean delivery. J Anaesthesiol
Clin Pharmacol 2011; 27:416-7.
[3]. Bradbury AW, Murie JA. Lymphatic system. In: Bailey and Love’s Short Practice of Surgery. 23rd edition, Russel RCG, Williams
NS, Blustrode CJK (Eds.), Arnold: London 2000:p.250-69.
[4]. Gaarenstroom KN, Kenter GG, Trimbos JB, Agous I, Amant F, Peters AA, et al. Postoperative complications after vulvectomy and
inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer 2003;13(4):522-7.
[5]. Pandhi RK, Sood A. Disease of arteries, veins and lymphatics. In: IADVL Textbook and Atlas of Dermatology. 2nd edition, Valia
RG, Valia AR (Eds.), Bhalani Publishing House: Mumbai 2001:p.576-95.
[6]. Mohan H, Bisht B, Goel P, Garg G. Vulval elephantiasis: a case report. Case Rep Infect Dis 2012; 2012:430745.
[7]. Schulman D, Beck LS, Roberts IM, Schwartz AM. Crohn’s disease of the vulva. Am J Gastroenterol 1987;82(12):1328-30.
[8]. Fenniche S, Mokni M, Haouet S, Ben Osman A. Vulvar Crohn disease: 3 cases. Ann Dermatol Venereol 1997;124(9):629-32.
[9]. Pal DK, Moulik D. Lymphangioma Circumscriptum of Vulva Due To Tuberculosis. The Internet Journal of Gynecology and
Obstetrics 2009:10.
[10]. Mu XC, Tran TA, Dupree M, Carlson JA. Acquired vulvar lymphangioma mimicking genital warts. A case report and review of
the literature.J Cuta Pathol 1999;26(3):150-
[11]. Miller TA, Wyatt LE, Rudkin GH. Staged skin and subcutaneous excision for lymphedema: a favorable report of long-term results.
Plast Reconstr Surg 1998;102(5):1486- 98; discussion 1499-501
[12]. Kim DI, Huh SH, Hwang JH, Joh JH. Excisional surgery for chronic advanced lymphedema. Surg Today 2004;34(2):134-7.

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Giant Vulvar Elephantiasis of Filarial Origin: A Rare Case Report

  • 1. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 14, Issue 11 Ver. II (Nov. 2015), PP 38-40 www.iosrjournals.org DOI: 10.9790/0853-141123840 www.iosrjournals.org 38 | Page Giant Vulvar Elephantiasis of Filarial Origin: A Rare Case Report Satish Kumar Ranjan4* , Mini Sinha3 , Nawal K Jha1 , D K Sinha2 , Amrisha Sharan4 1. Prof & Head , Department of general surgery , RIMS , Ranchi, India 2. Associate professor , department of general surgery ,RIMS , Ranchi, India 3. Senior resident , department of general surgery , RIMS , Ranchi, India 4. Junior resident , department of general surgery , RIMS , Ranchi ,India *Corresponding author: Dr Satish Kumar Ranjan Hostel no. 5 , room no. 43 RIMS , Bariatu , Ranchi-834009 Email id : docsatis48@gmail.com Abstract: Genital lymphedema is rare outside the endemic filariasis regions. Elephantiasis is the manifestation of chronic lymphedema. Involvement of limbs, trunk and male genitelia is common but elephantiasis of vulvar origin is rare even in endemic areas. we report a case of giant vulval elephantiasis in a young female. A 21 year old unmarried female presented with swelling of bilateral labia since 7 years with dragging pain and discomfort . Patient was managed by excision of filarial tumor with vulvoplasty and discharged uneventfully. Keywords: Elephantiasis , Lymphedema, Vulval , , Wuchereria bancrofti I. Introduction Genital elephantiasis is caused by a variety of infective and non infective causes leading to blockage of lymphatics. Vulvar elephentiasis is rare and it accounts of only 1-2% of total elephantiasis (1) . Greek terminology Esthioneme used to describe elephantiasis which means to eat and carries an idea something gnawed, eroded or ulcerated (2). Etiology of elephantiasis may be filarial , tubercular , chlamydial infection , post vulvectomy , post radiotherapy, after inguinal and pelvic lymph node dissection or idiopathic (3,4). Commonest infective Filariasis results from infection with Wuchereria bancrofti and Brugia malayi. Wuchereria bancrofti accounts for 90% of the case of human lymphatic filariasis. Nonlymphatic filarisis is caused by onchocera volvulus, loa loa or mansonella perstans. Lymphedema is due to accumulation of protein rich interstitial fluids, leads to proliferation of fibroblasts and mast cell , edema fluid organised progressively and fibrosis of the subcutaneous tissue giving rise to irreversible , firm and non pitting swelling. Hyperkeratosis, ruggosities , verrucous and condylomatous changes are features of long-standing lymph stasis and are collectively termed ‘elephantiasis”(5) II. Case Report A 21 year old unmarried girl presented in department of general surgery of Rajendra institute of medical sciences , Ranchi ,India with mild grade fever , dragging pain and swelling in genital area with difficulty in walking and working normally since 7years. Patient was also in significant psychological distress. There was no history of trauma , previous surgeries , radiotherapy, or chyluria .No history of swelling since childhood or lymphedema in family. All general and systemic examinations were within normal limit. On laboratories examinations Hb-10.5gm/dl , leukocyte count 10,400 cells/mm3, neutrophilia of 72%, lymphocyte 17% , eosinophil 08% , ESR 50mm in first hour was found. Patient was hepatitis B positive (HBsAg) with titer <6 IU/ml. On local examination bilateral vulval swelling was found [ fig. 1] . Size of swellings were 21x14 cm on left side and 7x4 cm on right side with illdefined margin , irregular bosselated surface, firm in consistency , freely mobile. There was no ulceration or lymphadenopathy. Cinical diagnosis of vulvar filariasis was made and total excision of tumor mass done under spinal anesthesia [fig. 2]. Two large irregular mass of weighs about 6 kg and 2 kg was excised [fig. 3]. Histopathological reports showed proliferation of stratified squamous epithelium showing acanthosis and increased junctional activity with Interlacing band of fibroblasts and collagen and perivascular mixed inflammatory infiltrate[fig. 4] . ZN and PAS staining was negative. Filarial antigen assay was positive. Pelvic ultrasonography was unremarkable.
  • 2. Giant vulvar elephantiasis of filarial origin: a rare case report DOI: 10.9790/0853-141123840 www.iosrjournals.org 39 | Page III. Discussion The term elephantiasis was first described by Celsius (30BC-50AD) (6). Lymphatic filariasis of external genitelia was first described in 1673. Vulval lymphedema can be a rare extraintestinal manifestation of Crohn’s disease (7,8). Differential diagnosis includes genital warts, lymphogranuloma, Lymphangioma circumscriptum, and fibro epithelial polyp, fungal infection, and carcinoma and angiomyxoma (9,10). Diagnosis of elephantiasis is mainly clinical and supported by histopathological examination. Neither microfilarae in blood nor adult worm in tissue can Found all the times (not sensitive). Treatment of filarial lymphedema is Diethylcarbamazine (DEC) in three divided doses of 6 mg/kg/day for 21 days kills adults and microfilarae. Leg elevation , elastic stocking , decongestive physiotherapy and maintenance of good skin care is also recommended. Surgical treatments includes excision of skin and subcutaneous tissue of involved part and primary closure of defect with normal adjacent skin. Partial thickness graft or rotation flap can be used if raw area is large. Surgical treatment is used only in extreme cases in order to reduce the weight of the affected organ, to help minimize the frequency of inflammatory attacks, to improve cosmesis, and to potentially reduce the risk of secondary angiosarcoma.(11,12). In our case patient came with large vulval swelling with difficulty in walk and work normally, after excision of mass we improved her life style and also provide good cosmosis which decreases her anxiety about future marital status. Rare presentation of our case evoks us to report the case. IV. Figure Figure 1 . Bilateral vulvar elephantiasis Figure 2. –Surgical excision of filarial tumor
  • 3. Giant vulvar elephantiasis of filarial origin: a rare case report DOI: 10.9790/0853-141123840 www.iosrjournals.org 40 | Page Figure 3- Specimen obtained after excision Figure 4. – Histopathological report showing acanthosis and increased junctional activity with Interlacing band of fibroblasts and collagen and perivascular mixed inflammatory infiltrate. V. Conclusion Although genital elephantiasis is rare in developed countries, it is still a challenge for tropics and subtropics. Genital elephantiasis significantly affect physical, social as well as mental status of the patient. So early detection and treatment of lymphedema is only option to prevent it. References [1]. Khanna NN, Joshi GK. Elephantiasis of female genitalia. Case peport. Plast Reconstr Surg 1971;48(4):379-81. [2]. Sharma K, Gupta S, Naithani U, Gupta S. Huge vulval elephantiasis Anesthetic management for caesarean delivery. J Anaesthesiol Clin Pharmacol 2011; 27:416-7. [3]. Bradbury AW, Murie JA. Lymphatic system. In: Bailey and Love’s Short Practice of Surgery. 23rd edition, Russel RCG, Williams NS, Blustrode CJK (Eds.), Arnold: London 2000:p.250-69. [4]. Gaarenstroom KN, Kenter GG, Trimbos JB, Agous I, Amant F, Peters AA, et al. Postoperative complications after vulvectomy and inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer 2003;13(4):522-7. [5]. Pandhi RK, Sood A. Disease of arteries, veins and lymphatics. In: IADVL Textbook and Atlas of Dermatology. 2nd edition, Valia RG, Valia AR (Eds.), Bhalani Publishing House: Mumbai 2001:p.576-95. [6]. Mohan H, Bisht B, Goel P, Garg G. Vulval elephantiasis: a case report. Case Rep Infect Dis 2012; 2012:430745. [7]. Schulman D, Beck LS, Roberts IM, Schwartz AM. Crohn’s disease of the vulva. Am J Gastroenterol 1987;82(12):1328-30. [8]. Fenniche S, Mokni M, Haouet S, Ben Osman A. Vulvar Crohn disease: 3 cases. Ann Dermatol Venereol 1997;124(9):629-32. [9]. Pal DK, Moulik D. Lymphangioma Circumscriptum of Vulva Due To Tuberculosis. The Internet Journal of Gynecology and Obstetrics 2009:10. [10]. Mu XC, Tran TA, Dupree M, Carlson JA. Acquired vulvar lymphangioma mimicking genital warts. A case report and review of the literature.J Cuta Pathol 1999;26(3):150- [11]. Miller TA, Wyatt LE, Rudkin GH. Staged skin and subcutaneous excision for lymphedema: a favorable report of long-term results. Plast Reconstr Surg 1998;102(5):1486- 98; discussion 1499-501 [12]. Kim DI, Huh SH, Hwang JH, Joh JH. Excisional surgery for chronic advanced lymphedema. Surg Today 2004;34(2):134-7.